ClinVar for Gene (Select 135941) - ClinVar

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Links from Gene

Items: 88

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302626	NM_001001659.3(OR2A14):c.778G>A (p.Ala260Thr)	OR2A14 (A260T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302625	NM_001001659.3(OR2A14):c.530T>A (p.Phe177Tyr)	OR2A14 (F177Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204993	NM_001001659.3(OR2A14):c.834C>A (p.Ser278Arg)	OR2A14 (S278R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204992	NM_001001659.3(OR2A14):c.628C>G (p.Leu210Val)	OR2A14 (L210V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204990	NM_001001659.3(OR2A14):c.192C>G (p.His64Gln)	OR2A14 (H64Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204989	NM_001001659.3(OR2A14):c.184C>T (p.Leu62Phe)	OR2A14 (L62F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204988	NM_001001659.3(OR2A14):c.182T>A (p.Phe61Tyr)	OR2A14 (F61Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204987	NM_001001659.3(OR2A14):c.146G>T (p.Cys49Phe)	OR2A14 (C49F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3148948	GRCh37/hg19 7q34-36.3(chr7:141690279-159119707)x3	ABCB8, ABCF2 +125 more	Copy number gain	See cases	GPathogenic
Select item 3062984	GRCh37/hg19 7q33-36.3(chr7:137456457-159119707)x3	ABCB8, ABCF2 +165 more	Copy number gain	not specified	GPathogenic
Select item 2685272	GRCh37/hg19 7q34-36.3(chr7:142099013-159119707)x1	CLCN1, RHEB +123 more	Copy number loss	not provided	GPathogenic
Select item 2685271	GRCh37/hg19 7q33-36.3(chr7:135639005-159119707)x1	ARHGEF35, KEL +169 more	Copy number loss	not provided	GPathogenic
Select item 2595321	NM_001001659.3(OR2A14):c.505G>A (p.Gly169Arg)	OR2A14 (G169R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2583057	GRCh37/hg19 7q34-36.1(chr7:140154317-152551638)x1	NDUFB2, NOBOX +125 more	Copy number loss	not provided	GPathogenic
Select item 2579171	GRCh38/hg38 7q34-36.3(chr7:138620939-159233475)x3	LOC129999716, LOC129999717 +847 more	Copy number gain	Neurodevelopmental disorder	GLikely pathogenic
Select item 2579170	GRCh38/hg38 7q33-36.3(chr7:137463392-159345973)x3	EPHA1-AS1, EPHB6 +888 more	Copy number gain	Neurodevelopmental disorder	GPathogenic
Select item 2547806	NM_001001659.3(OR2A14):c.346G>C (p.Val116Leu)	OR2A14 (V116L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545908	NM_001001659.3(OR2A14):c.106C>T (p.Leu36Phe)	OR2A14 (L36F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2522682	NM_001001659.3(OR2A14):c.613A>G (p.Ile205Val)	OR2A14 (I205V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521659	NM_001001659.3(OR2A14):c.260A>T (p.Gln87Leu)	OR2A14 (Q87L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474765	NM_001001659.3(OR2A14):c.817C>T (p.Leu273Phe)	OR2A14 (L273F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467888	NM_001001659.3(OR2A14):c.857C>T (p.Pro286Leu)	OR2A14 (P286L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462517	NM_001001659.3(OR2A14):c.655C>T (p.Arg219Cys)	OR2A14 (R219C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2457736	NM_001001659.3(OR2A14):c.109A>T (p.Thr37Ser)	OR2A14 (T37S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456483	NM_001001659.3(OR2A14):c.736G>A (p.Val246Met)	OR2A14 (V246M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454919	NM_001001659.3(OR2A14):c.139A>T (p.Ile47Phe)	OR2A14 (I47F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2425346	NC_000007.13:g.(?_130781014)_(150301047_?)del	CTAGE6, CTAGE8 +141 more	Deletion	not provided	GPathogenic
Select item 2398802	NM_001001659.3(OR2A14):c.667G>C (p.Ala223Pro)	OR2A14 (A223P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373914	NM_001001659.3(OR2A14):c.211T>C (p.Ser71Pro)	OR2A14 (S71P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316098	NM_001001659.3(OR2A14):c.877A>G (p.Asn293Asp)	OR2A14 (N293D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313499	NM_001001659.3(OR2A14):c.155G>C (p.Cys52Ser)	OR2A14 (C52S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2287253	NM_001001659.3(OR2A14):c.95C>T (p.Ala32Val)	OR2A14 (A32V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2274354	NM_001001659.3(OR2A14):c.413G>A (p.Arg138Lys)	OR2A14 (R138K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251891	NM_001001659.3(OR2A14):c.388C>T (p.Arg130Cys)	OR2A14 (R130C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234927	NM_001001659.3(OR2A14):c.202G>C (p.Val68Leu)	OR2A14 (V68L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209424	NM_001001659.3(OR2A14):c.404T>C (p.Met135Thr)	OR2A14 (M135T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1807754	GRCh37/hg19 7q32.3-36.1(chr7:131779213-149042734)x1	RAB19, RNY1 +123 more	Copy number loss	not provided	GPathogenic
Select item 1708459	GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1	AASS, ABCA13 +896 more	Copy number loss	See cases	GUncertain significance
Select item 1707419	GRCh37/hg19 7q35(chr7:143425718-144075390)x1	ARHGEF35, ARHGEF5 +16 more	Copy number loss	See cases	GUncertain significance
Select item 1703560	Single allele	CACNA2D1, CADPS2 +896 more	Complex	Ring chromosome 7	GPathogenic
Select item 1341257	GRCh37/hg19 7q33-36.3(chr7:133851002-159119707)x3	ABCB8, ABCF2 +186 more	Copy number gain	not provided	GPathogenic
Select item 1330183	GRCh37/hg19 7q33-35(chr7:133848099-145814115)x1	EPHA1, EPHB6 +105 more	Copy number loss	Hypertelorism +7 more	GPathogenic
Select item 973042	GRCh37/hg19 7q35-36.3(chr7:143107740-156886246)x3	ABCB8, ABCF2 +96 more	Copy number gain	not provided	Gnot provided
Select item 816507	GRCh37/hg19 7q32.3-36.3(chr7:131414604-159126310)x1	ABCB8, ABCF2 +190 more	Copy number loss	See cases	GPathogenic
Select item 815017	GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3	CHRM2, KRBA1 +295 more	Copy number gain	not provided	GPathogenic
Select item 688878	GRCh37/hg19 7q32.3-36.3(chr7:130592554-159119707)x3	OR2A25, OR2A42 +192 more	Copy number gain	not provided	GPathogenic
Select item 687979	GRCh37/hg19 7q34-35(chr7:141751875-147105208)x3	ARHGEF35, ARHGEF5 +44 more	Copy number gain	not provided	GUncertain significance
Select item 687739	GRCh37/hg19 7q35(chr7:143572320-144474990)x3	ARHGEF35, ARHGEF5 +16 more	Copy number gain	not provided	GUncertain significance
Select item 687427	GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3	PRSS1, PRSS37 +896 more	Copy number gain	not provided	GPathogenic
Select item 625550	GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220)	ABCB8, ABCF2 +229 more	Copy number gain	not provided	GPathogenic
Select item 563422	GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3	AASS, ABCB8 +436 more	Copy number gain	not provided	GPathogenic
Select item 563421	GRCh37/hg19 7q34-36.3(chr7:140133025-158982771)x1	ABCB8, ABCF2 +143 more	Copy number loss	not provided	GPathogenic
Select item 442966	GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1	ABCB8, ABCF2 +162 more	Copy number loss	See cases	GPathogenic
Select item 442834	GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3	AVL9, AZGP1 +896 more	Copy number gain	See cases	GPathogenic
Select item 442833	GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)	MCM7, MDFIC +896 more	Copy number gain	See cases	GPathogenic
Select item 442595	GRCh37/hg19 7q34-36.3(chr7:140636858-159119707)x1	ABCB8, ABCF2 +138 more	Copy number loss	See cases	GPathogenic
Select item 441751	GRCh37/hg19 7q33-36.3(chr7:136758593-159119707)x3	DGKI, DNAJB6 +166 more	Copy number gain	See cases	GPathogenic
Select item 226182	GRCh37/hg19 7q35(chr7:143342375-143913713)	ARHGEF35, CTAGE4 +11 more	Copy number gain	Abnormal esophagus morphology	GBenign
Select item 155687	GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3	PRKAG2, PRKAG2-AS1 +1052 more	Copy number gain	See cases	GPathogenic
Select item 155657	GRCh38/hg38 7q34-35(chr7:140061285-144622893)x3	TRBC1, TRBC2 +230 more	Copy number gain	See cases	GUncertain significance
Select item 155640	GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3	TRBV27, TRBV28 +1025 more	Copy number gain	See cases	GPathogenic
Select item 155173	GRCh38/hg38 7q35(chr7:143733925-144255312)x3	ARHGEF35, ARHGEF35-AS1 +20 more	Copy number gain	See cases	GUncertain significance
Select item 154735	GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3	LOC129389895, LOC129389896 +1046 more	Copy number gain	See cases	GPathogenic
Select item 153908	GRCh38/hg38 7q35(chr7:143728625-144176869)x1	CTAGE6, LOC129389908 +16 more	Copy number loss	See cases	Gconflicting data from submitters
Select item 152912	GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3	AASS, ABCB8 +1547 more	Copy number gain	See cases	GPathogenic
Select item 150974	GRCh38/hg38 7q35(chr7:143735880-144155736)x3	CTAGE6, LOC129389908 +15 more	Copy number gain	See cases	GLikely benign
Select item 150858	GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3	OR2A2, OR2A25 +1025 more	Copy number gain	See cases	GPathogenic
Select item 149975	GRCh38/hg38 7q33-36.1(chr7:135017687-148807400)x1	TRBC2, TRBD1 +455 more	Copy number loss	See cases	GPathogenic
Select item 149905	GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3	AASS, ABCB8 +1380 more	Copy number gain	See cases	GPathogenic
Select item 149558	GRCh38/hg38 7q35-36.1(chr7:143596735-150089125)x4	ACTR3C, ARHGEF35 +172 more	Copy number gain	See cases	GLikely pathogenic
Select item 149221	GRCh38/hg38 7q35(chr7:143560424-144169056)x3	CTAGE15, CTAGE6 +19 more	Copy number gain	See cases	GLikely benign
Select item 149061	GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1	LOC129999635, LOC129999636 +944 more	Copy number loss	See cases	GPathogenic
Select item 148181	GRCh38/hg38 7q34-36.3(chr7:141960861-159335866)x1	LOC129999721, LOC129999722 +707 more	Copy number loss	See cases	GPathogenic
Select item 147547	GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3	LOC123956257, LOC123956258 +2213 more	Copy number gain	See cases	GPathogenic
Select item 147398	GRCh38/hg38 7q33-36.2(chr7:137751200-154815582)x3	ABCB8, ABCF2 +692 more	Copy number gain	See cases	GPathogenic
Select item 146871	GRCh38/hg38 7q35(chr7:143735880-144409525)x3	ARHGEF35, ARHGEF35-AS1 +27 more	Copy number gain	See cases	GLikely benign
Select item 146155	GRCh38/hg38 7q35(chr7:143735739-144155939)x3	CTAGE6, LOC129389908 +15 more	Copy number gain	See cases	GBenign
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	CUL1, CUX1 +4737 more	Copy number loss	See cases	GPathogenic
Select item 144390	GRCh38/hg38 7q35(chr7:143735739-144254897)x3	ARHGEF35, ARHGEF35-AS1 +20 more	Copy number gain	See cases	GBenign
Select item 144163	GRCh38/hg38 7q34-35(chr7:141126407-145652221)x3	AGK, AGK-DT +192 more	Copy number gain	See cases	GPathogenic
Select item 60302	GRCh38/hg38 7q35-36.3(chr7:143884559-159282390)x1	LOC129999681, LOC129999682 +573 more	Copy number loss	See cases	GPathogenic
Select item 60300	GRCh38/hg38 7q34-36.3(chr7:140754198-159307523)x1	ABCB8, ABCF2 +737 more	Copy number loss	See cases	GPathogenic
Select item 60297	GRCh38/hg38 7q33-35(chr7:135414108-144140219)x1	ADCK2, AGK +373 more	Copy number loss	See cases	GPathogenic
Select item 59716	GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3	ABCB8, ABCF2 +908 more	Copy number gain	See cases	GPathogenic
Select item 57401	GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3	TRC-GCA9-3, TRC-GCA9-4 +1019 more	Copy number gain	See cases	GPathogenic
Select item 57215	GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3	ABCB8, ABCF2 +1176 more	Copy number gain	See cases	GPathogenic
Select item 57118	GRCh38/hg38 7q35-36.1(chr7:143884559-152674271)x1	ABCB8, ABCF2 +358 more	Copy number loss	See cases	GPathogenic
Select item 57046	GRCh38/hg38 7q34-35(chr7:142578948-144254897)x1	ARHGEF35, ARHGEF35-AS1 +110 more	Copy number loss	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 88