54949[geneid] - ClinVar - NCBI

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VariationLocation		Gene(s)	Protein change	Condition(s)	Clinical significance (Last reviewed)	Review status
Select item 1504571.	GRCh38/hg38 11q12.2(chr11:61181337-61516830)x3 GRCh37: Chr11:60948809-61284302 GRCh38: Chr11:61181337-61516830	CPSF7, CYB561A3, DDB1, LOC121392920, LOC126861223, LOC126861224, LRRC10B, MIR4488, PGA3, PGA4, PGA5, PPP1R32, SDHAF2, SYT7, TKFC, TMEM138, TMEM216, VWCE		See cases	Uncertain significance (Sep 21, 2012)	no assertion criteria provided
Select item 1468192.	GRCh38/hg38 11q12.2(chr11:61409529-61821159)x3 GRCh37: Chr11:61177001-61588631 GRCh38: Chr11:61409529-61821159	CPSF7, DAGLA, FADS1, FADS2, FEN1, LOC101927495, LOC111818968, LOC121392920, LOC121392921, LOC124489747, LOC126861225, LRRC10B, MIR1908, MIR4488, MIR611, MYRF, MYRF-AS1, PPP1R32, SDHAF2, SYT7, TMEM258		See cases	Likely benign (Nov 30, 2010)	no assertion criteria provided
Select item 12662543.	Single allele GRCh37: Chr11:61197461 GRCh38: Chr11:61429989	SDHAF2		not provided	Benign (Jun 23, 2018)	criteria provided, single submitter
Select item 5137394.	NM_017841.2(SDHAF2):c.-50G>T GRCh37: Chr11:61197569 GRCh38: Chr11:61430097	SDHAF2		not specified	Likely benign (Nov 24, 2017)	criteria provided, single submitter
Select item 8789875.	NM_017841.2(SDHAF2):c.-29G>A GRCh37: Chr11:61197590 GRCh38: Chr11:61430118	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 5079826.	NM_017841.4(SDHAF2):c.-11A>G GRCh37: Chr11:61197608 GRCh38: Chr11:61430136	SDHAF2		not specified	Likely benign (Mar 20, 2017)	criteria provided, single submitter
Select item 17510017.	NM_017841.4(SDHAF2):c.-5G>A GRCh37: Chr11:61197614 GRCh38: Chr11:61430142	SDHAF2		Hereditary cancer-predisposing syndrome	Uncertain significance (Oct 15, 2021)	criteria provided, single submitter
Select item 8261218.	NM_017841.4(SDHAF2):c.-5G>T GRCh37: Chr11:61197614 GRCh38: Chr11:61430142	SDHAF2		Hereditary cancer-predisposing syndrome	Uncertain significance (Apr 26, 2018)	criteria provided, single submitter
Select item 3921109.	NM_017841.4(SDHAF2):c.-1A>C GRCh37: Chr11:61197618 GRCh38: Chr11:61430146	SDHAF2		Paragangliomas 2, Hereditary cancer-predisposing syndrome, not provided	Conflicting interpretations of pathogenicity (Mar 20, 2023)	criteria provided, conflicting interpretations
Select item 41160910.	NM_017841.4(SDHAF2):c.2T>C (p.Met1Thr) GRCh37: Chr11:61197620 GRCh38: Chr11:61430148	SDHAF2	M1T	Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 3, 2022)	criteria provided, multiple submitters, no conflicts
Select item 95157911.	NM_017841.4(SDHAF2):c.3G>A (p.Met1Ile) GRCh37: Chr11:61197621 GRCh38: Chr11:61430149	SDHAF2	M1I	Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Aug 26, 2021)	criteria provided, multiple submitters, no conflicts
Select item 244852012.	NM_017841.4(SDHAF2):c.4G>T (p.Ala2Ser) GRCh37: Chr11:61197622 GRCh38: Chr11:61430150	SDHAF2	A2S	Hereditary cancer-predisposing syndrome	Uncertain significance (Dec 19, 2022)	criteria provided, single submitter
Select item 206397713.	NM_017841.4(SDHAF2):c.5C>T (p.Ala2Val) GRCh37: Chr11:61197623 GRCh38: Chr11:61430151	SDHAF2	A2V	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Feb 24, 2022)	criteria provided, single submitter
Select item 48641114.	NM_017841.4(SDHAF2):c.6G>T (p.Ala2=) GRCh37: Chr11:61197624 GRCh38: Chr11:61430152	SDHAF2		Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Likely benign (Aug 23, 2022)	criteria provided, multiple submitters, no conflicts
Select item 46383215.	NM_017841.4(SDHAF2):c.6G>A (p.Ala2=) GRCh37: Chr11:61197624 GRCh38: Chr11:61430152	SDHAF2		Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome, not provided	Likely benign (Oct 13, 2022)	criteria provided, multiple submitters, no conflicts
Select item 48641516.	NM_017841.4(SDHAF2):c.7G>A (p.Val3Met) GRCh37: Chr11:61197625 GRCh38: Chr11:61430153	SDHAF2	V3M	Hereditary cancer-predisposing syndrome	Uncertain significance (Jun 13, 2019)	criteria provided, single submitter
Select item 41160717.	NM_017841.4(SDHAF2):c.7G>T (p.Val3Leu) GRCh37: Chr11:61197625 GRCh38: Chr11:61430153	SDHAF2	V3L	Hereditary cancer-predisposing syndrome, not provided, Hereditary pheochromocytoma-paraganglioma	Conflicting interpretations of pathogenicity (Mar 7, 2023)	criteria provided, conflicting interpretations
Select item 94847318.	NM_017841.4(SDHAF2):c.8T>C (p.Val3Ala) GRCh37: Chr11:61197626 GRCh38: Chr11:61430154	SDHAF2	V3A	Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 13, 2022)	criteria provided, multiple submitters, no conflicts
Select item 244851919.	NM_017841.4(SDHAF2):c.9G>T (p.Val3=) GRCh37: Chr11:61197627 GRCh38: Chr11:61430155	SDHAF2		Hereditary cancer-predisposing syndrome	Uncertain significance (Dec 9, 2022)	criteria provided, single submitter
Select item 217749420.	NM_017841.4(SDHAF2):c.9G>C (p.Val3=) GRCh37: Chr11:61197627 GRCh38: Chr11:61430155	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Apr 20, 2022)	criteria provided, single submitter
Select item 161551321.	NM_017841.4(SDHAF2):c.9G>A (p.Val3=) GRCh37: Chr11:61197627 GRCh38: Chr11:61430155	SDHAF2		Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Likely benign (Aug 15, 2022)	criteria provided, multiple submitters, no conflicts
Select item 104470422.	NM_017841.4(SDHAF2):c.10T>G (p.Ser4Ala) GRCh37: Chr11:61197628 GRCh38: Chr11:61430156	SDHAF2	S4A	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Aug 27, 2021)	criteria provided, single submitter
Select item 151035423.	NM_017841.4(SDHAF2):c.11C>T (p.Ser4Phe) GRCh37: Chr11:61197629 GRCh38: Chr11:61430157	SDHAF2	S4F	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 24, 2022)	criteria provided, single submitter
Select item 64737624.	NM_017841.4(SDHAF2):c.11C>G (p.Ser4Cys) GRCh37: Chr11:61197629 GRCh38: Chr11:61430157	SDHAF2	S4C	Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Aug 6, 2022)	criteria provided, multiple submitters, no conflicts
Select item 176938125.	NM_017841.4(SDHAF2):c.12T>C (p.Ser4=) GRCh37: Chr11:61197630 GRCh38: Chr11:61430158	SDHAF2		Hereditary cancer-predisposing syndrome	Likely benign (May 26, 2019)	criteria provided, single submitter
Select item 111961026.	NM_017841.4(SDHAF2):c.12T>A (p.Ser4=) GRCh37: Chr11:61197630 GRCh38: Chr11:61430158	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Sep 3, 2020)	criteria provided, single submitter
Select item 41161027.	NM_017841.4(SDHAF2):c.13A>G (p.Thr5Ala) GRCh37: Chr11:61197631 GRCh38: Chr11:61430159	SDHAF2	T5A	Hereditary cancer-predisposing syndrome, not provided, Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 31, 2022)	criteria provided, multiple submitters, no conflicts
Select item 96094728.	NM_017841.4(SDHAF2):c.14C>T (p.Thr5Ile) GRCh37: Chr11:61197632 GRCh38: Chr11:61430160	SDHAF2	T5I	Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Aug 30, 2022)	criteria provided, multiple submitters, no conflicts
Select item 41679629.	NM_017841.4(SDHAF2):c.15A>G (p.Thr5=) GRCh37: Chr11:61197633 GRCh38: Chr11:61430161	SDHAF2		Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Benign/Likely benign (Nov 4, 2022)	criteria provided, multiple submitters, no conflicts
Select item 96230430.	NM_017841.4(SDHAF2):c.17T>C (p.Val6Ala) GRCh37: Chr11:61197635 GRCh38: Chr11:61430163	SDHAF2	V6A	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 25, 2019)	criteria provided, single submitter
Select item 196454331.	NM_017841.4(SDHAF2):c.18G>C (p.Val6=) GRCh37: Chr11:61197636 GRCh38: Chr11:61430164	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Apr 29, 2022)	criteria provided, single submitter
Select item 70030032.	NM_017841.4(SDHAF2):c.18G>A (p.Val6=) GRCh37: Chr11:61197636 GRCh38: Chr11:61430164	SDHAF2		Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Likely benign (Sep 27, 2018)	criteria provided, multiple submitters, no conflicts
Select item 205564233.	NM_017841.4(SDHAF2):c.19T>C (p.Phe7Leu) GRCh37: Chr11:61197637 GRCh38: Chr11:61430165	SDHAF2	F7L	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Mar 5, 2022)	criteria provided, single submitter
Select item 199679434.	NM_017841.4(SDHAF2):c.19T>G (p.Phe7Val) GRCh37: Chr11:61197637 GRCh38: Chr11:61430165	SDHAF2	F7V	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (May 20, 2022)	criteria provided, single submitter
Select item 214924335.	NM_017841.4(SDHAF2):c.21C>A (p.Phe7Leu) GRCh37: Chr11:61197639 GRCh38: Chr11:61430167	SDHAF2	F7L	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 17, 2022)	criteria provided, single submitter
Select item 41679436.	NM_017841.4(SDHAF2):c.21C>T (p.Phe7=) GRCh37: Chr11:61197639 GRCh38: Chr11:61430167	SDHAF2		Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Likely benign (Nov 3, 2022)	criteria provided, multiple submitters, no conflicts
Select item 178927437.	NM_017841.4(SDHAF2):c.22T>C (p.Ser8Pro) GRCh37: Chr11:61197640 GRCh38: Chr11:61430168	SDHAF2	S8P	Hereditary cancer-predisposing syndrome	Likely benign (Sep 26, 2022)	criteria provided, single submitter
Select item 178927338.	NM_017841.4(SDHAF2):c.22T>A (p.Ser8Thr) GRCh37: Chr11:61197640 GRCh38: Chr11:61430168	SDHAF2	S8T	Hereditary cancer-predisposing syndrome	Uncertain significance (May 7, 2022)	criteria provided, single submitter
Select item 179070239.	NM_017841.4(SDHAF2):c.23C>G (p.Ser8Trp) GRCh37: Chr11:61197641 GRCh38: Chr11:61430169	SDHAF2	S8W	Hereditary cancer-predisposing syndrome	Uncertain significance (Feb 7, 2022)	criteria provided, single submitter
Select item 137288140.	NM_017841.4(SDHAF2):c.23C>T (p.Ser8Leu) GRCh37: Chr11:61197641 GRCh38: Chr11:61430169	SDHAF2	S8L	Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Uncertain significance (Nov 27, 2021)	criteria provided, multiple submitters, no conflicts
Select item 82121741.	NM_017841.4(SDHAF2):c.23C>A (p.Ser8Ter) GRCh37: Chr11:61197641 GRCh38: Chr11:61430169	SDHAF2	S8*	Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Conflicting interpretations of pathogenicity (Aug 16, 2022)	criteria provided, conflicting interpretations
Select item 179223242.	NM_017841.4(SDHAF2):c.24G>C (p.Ser8=) GRCh37: Chr11:61197642 GRCh38: Chr11:61430170	SDHAF2		Hereditary cancer-predisposing syndrome	Likely benign (Jan 31, 2020)	criteria provided, single submitter
Select item 109246543.	NM_017841.4(SDHAF2):c.24G>T (p.Ser8=) GRCh37: Chr11:61197642 GRCh38: Chr11:61430170	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Apr 15, 2022)	criteria provided, single submitter
Select item 48640944.	NM_017841.4(SDHAF2):c.24G>A (p.Ser8=) GRCh37: Chr11:61197642 GRCh38: Chr11:61430170	SDHAF2		Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Likely benign (Sep 3, 2022)	criteria provided, multiple submitters, no conflicts
Select item 46382045.	NM_017841.4(SDHAF2):c.25A>G (p.Thr9Ala) GRCh37: Chr11:61197643 GRCh38: Chr11:61430171	SDHAF2	T9A	Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Conflicting interpretations of pathogenicity (Jun 10, 2022)	criteria provided, conflicting interpretations
Select item 146083446.	NM_017841.4(SDHAF2):c.26C>T (p.Thr9Ile) GRCh37: Chr11:61197644 GRCh38: Chr11:61430172	SDHAF2	T9I	Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Uncertain significance (Nov 1, 2022)	criteria provided, multiple submitters, no conflicts
Select item 145184447.	NM_017841.4(SDHAF2):c.28del (p.Ser10fs) GRCh37: Chr11:61197645 GRCh38: Chr11:61430173	SDHAF2	S10fs	Hereditary pheochromocytoma-paraganglioma	Pathogenic (Aug 14, 2022)	criteria provided, single submitter
Select item 104650148.	NM_017841.4(SDHAF2):c.28T>A (p.Ser10Thr) GRCh37: Chr11:61197646 GRCh38: Chr11:61430174	SDHAF2	S10T	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Sep 2, 2021)	criteria provided, single submitter
Select item 244852149.	NM_017841.4(SDHAF2):c.29C>G (p.Ser10Trp) GRCh37: Chr11:61197647 GRCh38: Chr11:61430175	SDHAF2	S10W	Hereditary cancer-predisposing syndrome	Uncertain significance (Dec 24, 2022)	criteria provided, single submitter
Select item 82249650.	NM_017841.4(SDHAF2):c.29del (p.Ser10fs) GRCh37: Chr11:61197647 GRCh38: Chr11:61430175	SDHAF2	S10fs	Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Conflicting interpretations of pathogenicity (Mar 19, 2022)	criteria provided, conflicting interpretations
Select item 65300051.	NM_017841.4(SDHAF2):c.29C>T (p.Ser10Leu) GRCh37: Chr11:61197647 GRCh38: Chr11:61430175	SDHAF2	S10L	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 24, 2022)	criteria provided, single submitter
Select item 166805252.	NM_017841.4(SDHAF2):c.30G>C (p.Ser10=) GRCh37: Chr11:61197648 GRCh38: Chr11:61430176	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Dec 31, 2020)	criteria provided, single submitter
Select item 215844853.	NM_017841.4(SDHAF2):c.32C>A (p.Ser11Ter) GRCh37: Chr11:61197650 GRCh38: Chr11:61430178	SDHAF2	S11*	Hereditary pheochromocytoma-paraganglioma	Pathogenic (Aug 25, 2022)	criteria provided, single submitter
Select item 139215054.	NM_017841.4(SDHAF2):c.32C>G (p.Ser11Trp) GRCh37: Chr11:61197650 GRCh38: Chr11:61430178	SDHAF2	S11W	Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Uncertain significance (Oct 11, 2022)	criteria provided, multiple submitters, no conflicts
Select item 46382555.	NM_017841.4(SDHAF2):c.32C>T (p.Ser11Leu) GRCh37: Chr11:61197650 GRCh38: Chr11:61430178	SDHAF2	S11L	not provided, Paragangliomas 2, Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Likely benign (Oct 26, 2022)	criteria provided, multiple submitters, no conflicts
Select item 173105156.	NM_017841.4(SDHAF2):c.33G>T (p.Ser11=) GRCh37: Chr11:61197651 GRCh38: Chr11:61430179	SDHAF2		Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Likely benign (Aug 10, 2022)	criteria provided, multiple submitters, no conflicts
Select item 173102957.	NM_017841.4(SDHAF2):c.33G>A (p.Ser11=) GRCh37: Chr11:61197651 GRCh38: Chr11:61430179	SDHAF2		Hereditary cancer-predisposing syndrome	Likely benign (Oct 12, 2021)	criteria provided, single submitter
Select item 173102658.	NM_017841.4(SDHAF2):c.33del (p.Ser11_Leu12insTer) GRCh37: Chr11:61197651 GRCh38: Chr11:61430179	SDHAF2		Hereditary cancer-predisposing syndrome	Uncertain significance (Apr 18, 2022)	criteria provided, single submitter
Select item 114239059.	NM_017841.4(SDHAF2):c.34C>T (p.Leu12=) GRCh37: Chr11:61197652 GRCh38: Chr11:61430180	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Nov 4, 2019)	criteria provided, single submitter
Select item 171884560.	NM_017841.4(SDHAF2):c.35T>A (p.Leu12Gln) GRCh37: Chr11:61197653 GRCh38: Chr11:61430181	SDHAF2	L12Q	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Sep 15, 2022)	criteria provided, single submitter
Select item 66578761.	NM_017841.4(SDHAF2):c.35T>C (p.Leu12Pro) GRCh37: Chr11:61197653 GRCh38: Chr11:61430181	SDHAF2	L12P	Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Nov 2, 2021)	criteria provided, multiple submitters, no conflicts
Select item 199150462.	NM_017841.4(SDHAF2):c.36G>T (p.Leu12=) GRCh37: Chr11:61197654 GRCh38: Chr11:61430182	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 5, 2022)	criteria provided, single submitter
Select item 202073663.	NM_017841.4(SDHAF2):c.36+1G>A GRCh37: Chr11:61197655 GRCh38: Chr11:61430183	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely pathogenic (Jul 30, 2022)	criteria provided, single submitter
Select item 173308864.	NM_017841.4(SDHAF2):c.36+1G>T GRCh37: Chr11:61197655 GRCh38: Chr11:61430183	SDHAF2		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 7, 2022)	criteria provided, single submitter
Select item 65569365.	NM_017841.4(SDHAF2):c.36+5G>A GRCh37: Chr11:61197659 GRCh38: Chr11:61430187	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Jun 13, 2020)	criteria provided, single submitter
Select item 142141666.	NM_017841.4(SDHAF2):c.36+6G>A GRCh37: Chr11:61197660 GRCh38: Chr11:61430188	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Feb 7, 2022)	criteria provided, single submitter
Select item 107755167.	NM_017841.4(SDHAF2):c.36+6GA[2] GRCh37: Chr11:61197660-61197663 GRCh38: Chr11:61430188-61430191	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Sep 1, 2022)	criteria provided, single submitter
Select item 154620368.	NM_017841.4(SDHAF2):c.36+7_36+9del GRCh37: Chr11:61197661-61197663 GRCh38: Chr11:61430189-61430191	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Jul 25, 2021)	criteria provided, single submitter
Select item 150623669.	NM_017841.4(SDHAF2):c.36+9A>T GRCh37: Chr11:61197663 GRCh38: Chr11:61430191	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Aug 22, 2022)	criteria provided, single submitter
Select item 24121770.	NM_017841.4(SDHAF2):c.36+10G>A GRCh37: Chr11:61197664 GRCh38: Chr11:61430192	SDHAF2		Hereditary pheochromocytoma-paraganglioma, Paragangliomas 2, not specified	Benign/Likely benign (Oct 20, 2022)	criteria provided, multiple submitters, no conflicts
Select item 161151671.	NM_017841.4(SDHAF2):c.36+11A>C GRCh37: Chr11:61197665 GRCh38: Chr11:61430193	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Oct 17, 2021)	criteria provided, single submitter
Select item 219721272.	NM_017841.4(SDHAF2):c.36+12G>A GRCh37: Chr11:61197666 GRCh38: Chr11:61430194	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Sep 23, 2022)	criteria provided, single submitter
Select item 196242873.	NM_017841.4(SDHAF2):c.36+12G>C GRCh37: Chr11:61197666 GRCh38: Chr11:61430194	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Sep 5, 2022)	criteria provided, single submitter
Select item 212991874.	NM_017841.4(SDHAF2):c.36+14A>T GRCh37: Chr11:61197668 GRCh38: Chr11:61430196	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Apr 24, 2022)	criteria provided, single submitter
Select item 166002675.	NM_017841.4(SDHAF2):c.36+14A>G GRCh37: Chr11:61197668 GRCh38: Chr11:61430196	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Sep 15, 2021)	criteria provided, single submitter
Select item 199004476.	NM_017841.4(SDHAF2):c.36+16G>A GRCh37: Chr11:61197670 GRCh38: Chr11:61430198	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Jun 24, 2022)	criteria provided, single submitter
Select item 26094377.	NM_017841.4(SDHAF2):c.36+17T>C GRCh37: Chr11:61197671 GRCh38: Chr11:61430199	SDHAF2		Hereditary pheochromocytoma-paraganglioma, not specified	Benign/Likely benign (Oct 31, 2022)	criteria provided, multiple submitters, no conflicts
Select item 163581378.	NM_017841.4(SDHAF2):c.36+19C>G GRCh37: Chr11:61197673 GRCh38: Chr11:61430201	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Oct 13, 2022)	criteria provided, single submitter
Select item 120291179.	NM_017841.4(SDHAF2):c.36+284C>T GRCh37: Chr11:61197938 GRCh38: Chr11:61430466	SDHAF2		not provided	Likely benign (Jun 17, 2019)	criteria provided, single submitter
Select item 120020780.	NM_017841.4(SDHAF2):c.37-176G>A GRCh37: Chr11:61204921 GRCh38: Chr11:61437449	SDHAF2		not provided	Likely benign (Jun 23, 2018)	criteria provided, single submitter
Select item 219061481.	NM_017841.4(SDHAF2):c.37-20T>G GRCh37: Chr11:61205077 GRCh38: Chr11:61437605	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Sep 15, 2022)	criteria provided, single submitter
Select item 157130082.	NM_017841.4(SDHAF2):c.37-18G>A GRCh37: Chr11:61205079 GRCh38: Chr11:61437607	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Oct 5, 2022)	criteria provided, single submitter
Select item 63938483.	NC_000011.9:g.(?_61205087)_(61213553_?)dup GRCh37: Chr11:61205087-61213553 GRCh38: Chr11:61437615-61446081	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Oct 30, 2019)	criteria provided, single submitter
Select item 101477984.	NM_017841.4(SDHAF2):c.37-8del GRCh37: Chr11:61205089 GRCh38: Chr11:61437617	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Aug 30, 2021)	criteria provided, single submitter
Select item 46382685.	NM_017841.4(SDHAF2):c.37-7A>G GRCh37: Chr11:61205090 GRCh38: Chr11:61437618	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Jul 19, 2020)	criteria provided, single submitter
Select item 167499786.	NM_017841.4(SDHAF2):c.37-6T>C GRCh37: Chr11:61205091 GRCh38: Chr11:61437619	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Likely benign (Jul 15, 2021)	criteria provided, single submitter
Select item 203361387.	NM_017841.4(SDHAF2):c.37-5T>C GRCh37: Chr11:61205092 GRCh38: Chr11:61437620	SDHAF2		Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Aug 8, 2022)	criteria provided, single submitter
Select item 106805488.	NM_017841.4(SDHAF2):c.37-2A>G GRCh37: Chr11:61205095 GRCh38: Chr11:61437623	SDHAF2		Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Likely pathogenic (Jul 11, 2022)	criteria provided, multiple submitters, no conflicts
Select item 80667889.	NM_017841.4(SDHAF2):c.37-1G>C GRCh37: Chr11:61205096 GRCh38: Chr11:61437624	SDHAF2		Hereditary pheochromocytoma-paraganglioma, not provided, Hereditary cancer-predisposing syndrome, Paragangliomas 2	Pathogenic/Likely pathogenic (Dec 16, 2022)	criteria provided, multiple submitters, no conflicts
Select item 95529190.	NM_017841.4(SDHAF2):c.37A>G (p.Met13Val) GRCh37: Chr11:61205097 GRCh38: Chr11:61437625	SDHAF2	M13V	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Aug 31, 2021)	criteria provided, single submitter
Select item 48640591.	NM_017841.4(SDHAF2):c.37A>T (p.Met13Leu) GRCh37: Chr11:61205097 GRCh38: Chr11:61437625	SDHAF2	M13L	Hereditary cancer-predisposing syndrome, Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Sep 1, 2021)	criteria provided, multiple submitters, no conflicts
Select item 98278492.	NM_017841.4(SDHAF2):c.42_45del (p.Ala15fs) GRCh37: Chr11:61205098-61205101 GRCh38: Chr11:61437626-61437629	SDHAF2	A15fs	Paragangliomas 2	Likely pathogenic (Jan 1, 2019)	criteria provided, single submitter
Select item 142804893.	NM_017841.4(SDHAF2):c.40C>T (p.Leu14Phe) GRCh37: Chr11:61205100 GRCh38: Chr11:61437628	SDHAF2	L14F	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Jul 19, 2022)	criteria provided, single submitter
Select item 85863394.	NM_017841.4(SDHAF2):c.43G>C (p.Ala15Pro) GRCh37: Chr11:61205103 GRCh38: Chr11:61437631	SDHAF2	A15P	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Sep 1, 2021)	criteria provided, single submitter
Select item 53250595.	NM_017841.4(SDHAF2):c.43G>T (p.Ala15Ser) GRCh37: Chr11:61205103 GRCh38: Chr11:61437631	SDHAF2	A15S	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Aug 29, 2022)	criteria provided, single submitter
Select item 174181296.	NM_017841.4(SDHAF2):c.45T>C (p.Ala15=) GRCh37: Chr11:61205105 GRCh38: Chr11:61437633	SDHAF2		Hereditary cancer-predisposing syndrome	Likely benign (Nov 10, 2020)	criteria provided, single submitter
Select item 95619797.	NM_017841.4(SDHAF2):c.46C>G (p.Leu16Val) GRCh37: Chr11:61205106 GRCh38: Chr11:61437634	SDHAF2	L16V	Hereditary pheochromocytoma-paraganglioma	Uncertain significance (Jul 22, 2019)	criteria provided, single submitter
Select item 82510998.	NM_017841.4(SDHAF2):c.46C>T (p.Leu16=) GRCh37: Chr11:61205106 GRCh38: Chr11:61437634	SDHAF2		Hereditary pheochromocytoma-paraganglioma, Hereditary cancer-predisposing syndrome	Likely benign (Aug 3, 2022)	criteria provided, multiple submitters, no conflicts
Select item 174395599.	NM_017841.4(SDHAF2):c.48G>A (p.Leu16=) GRCh37: Chr11:61205108 GRCh38: Chr11:61437636	SDHAF2		Hereditary cancer-predisposing syndrome	Likely benign (Mar 13, 2020)	criteria provided, single submitter
Select item 1744674100.	NM_017841.4(SDHAF2):c.49T>C (p.Ser17Pro) GRCh37: Chr11:61205109 GRCh38: Chr11:61437637	SDHAF2	S17P	Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 22, 2020)	criteria provided, single submitter

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