ClinVar for Gene (Select 10800) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270718	NM_006639.4(CYSLTR1):c.758G>A (p.Arg253His)	CYSLTR1 (R253H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270717	NM_006639.4(CYSLTR1):c.487C>G (p.Pro163Ala)	CYSLTR1 (P163A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270716	NM_006639.4(CYSLTR1):c.290G>A (p.Arg97His)	CYSLTR1 (R97H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242589	GRCh38/hg38 Xp22.33-q28(chrX:2757837-156030895)x2	LOC130068417, LOC130068418 +2599 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 3079800	NM_006639.4(CYSLTR1):c.796C>T (p.Pro266Ser)	CYSLTR1 (P266S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079799	NM_006639.4(CYSLTR1):c.781C>T (p.His261Tyr)	CYSLTR1 (H261Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079796	NM_006639.4(CYSLTR1):c.712G>A (p.Val238Met)	CYSLTR1 (V238M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079795	NM_006639.4(CYSLTR1):c.49A>C (p.Thr17Pro)	CYSLTR1 (T17P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079794	NM_006639.4(CYSLTR1):c.1004G>A (p.Cys335Tyr)	CYSLTR1 (C335Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062482	GRCh37/hg19 Xq11.1-21.1(chrX:61877278-79122848)	ABCB7, AMER1 +92 more	Copy number gain	not specified	GPathogenic
Select item 3062468	GRCh37/hg19 Xq13.1-22.1(chrX:68040342-100863081)	ABCB7, APOOL +121 more	Copy number gain	not specified	GPathogenic
Select item 3024654	GRCh37/hg19 Xq12-28(chrX:67292994-155240074)x3	CPXCR1, MAGEE2 +488 more	Copy number gain	not provided	GPathogenic
Select item 2685711	GRCh37/hg19 Xq13.2-21.31(chrX:73620711-90395211)x1	ABCB7, APOOL +39 more	Copy number loss	not provided	GPathogenic
Select item 2684996	GRCh37/hg19 Xq21.1-24(chrX:77212972-118576590)x3	ACSL4, AGTR2 +159 more	Copy number gain	not provided	GPathogenic
Select item 2660971	NM_006639.4(CYSLTR1):c.361C>T (p.Arg121Trp)	CYSLTR1 (R121W)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2660970	NM_006639.4(CYSLTR1):c.882A>G (p.Leu294=)	CYSLTR1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2607522	NM_006639.4(CYSLTR1):c.349A>G (p.Met117Val)	CYSLTR1 (M117V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559516	NM_006639.4(CYSLTR1):c.934C>G (p.His312Asp)	CYSLTR1 (H312D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537300	NM_006639.4(CYSLTR1):c.236G>T (p.Arg79Leu)	CYSLTR1 (R79L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529735	NM_006639.4(CYSLTR1):c.288C>G (p.Cys96Trp)	CYSLTR1 (C96W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527921	NM_006639.4(CYSLTR1):c.454A>T (p.Ile152Phe)	CYSLTR1 (I152F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527859	NM_006639.4(CYSLTR1):c.455T>A (p.Ile152Asn)	CYSLTR1 (I152N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2506546	GRCh37/hg19 Xp22.33-q28(chrX:200855-155240074)	ABCB7, ABCD1 +818 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 2381156	NM_006639.4(CYSLTR1):c.733A>T (p.Ser245Cys)	CYSLTR1 (S245C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334711	NM_006639.4(CYSLTR1):c.860A>G (p.Asn287Ser)	CYSLTR1 (N287S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301724	NM_006639.4(CYSLTR1):c.16A>T (p.Asn6Tyr)	CYSLTR1 (N6Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272583	NM_006639.4(CYSLTR1):c.65G>A (p.Arg22His)	CYSLTR1 (R22H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809226	GRCh37/hg19 Xq21.1(chrX:77544318-78390511)x3	CYSLTR1, LPAR4 +2 more	Copy number gain	not provided	GUncertain significance
Select item 1710513	GRCh37/hg19 Xq21.1-24(chrX:76794355-119282836)x3	CAPN6, CENPI +176 more	Copy number gain	not provided	GPathogenic
Select item 1707442	GRCh37/hg19 Xp22.2-q28(chrX:11522765-155233731)x1	ABCB7, ABCD1 +790 more	Copy number loss	See cases	GPathogenic
Select item 1704345	GRCh37/hg19 Xp22.33-q28(chrX:61545-155226048)x2	ABCB7, ABCD1 +818 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 1703584	GRCh37/hg19 Xq11.1-28(chrX:62685885-155233731)	ABCB7, ABCD1 +501 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703580	GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	ABCB7, ABCD1 +819 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703579	GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	AKAP14, CT47A11 +819 more	Copy number gain	Hypotonia +2 more	GPathogenic
Select item 1526821	GRCh37/hg19 Xq21.1(chrX:77577385-77720021)	CYSLTR1	Copy number loss	not specified	GUncertain significance
Select item 1526820	GRCh37/hg19 Xq21.1(chrX:77353716-77736775)	CYSLTR1, PGK1 +1 more	Copy number gain	not specified	GUncertain significance
Select item 1526819	GRCh37/hg19 Xq21.1(chrX:77212971-77537309)	ATP7A, CYSLTR1 +3 more	Copy number gain	not specified	GUncertain significance
Select item 1526815	GRCh37/hg19 Xq13.2-21.31(chrX:72095006-88455505)	APOOL, ABCB7 +49 more	Copy number gain	not specified	GUncertain significance
Select item 1526804	GRCh37/hg19 Xq11.1-21.1(chrX:61974855-79123671)	AWAT1, AWAT2 +92 more	Copy number gain	not specified	GPathogenic
Select item 1526803	GRCh37/hg19 Xq11.1-21.1(chrX:61877278-79123671)	NALF2, NAP1L2 +92 more	Copy number gain	not specified	GPathogenic
Select item 1341233	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	RADX, RAI2 +818 more	Copy number loss	not provided	GPathogenic
Select item 1341223	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3	GPM6B, KLHL15 +818 more	Copy number gain	not provided	GPathogenic
Select item 1340471	GRCh37/hg19 Xq21.1(chrX:77442685-77848108)x2	CYSLTR1	Copy number gain	not provided	GLikely benign
Select item 1184285	NC_000023.11:g.77957506_78280549dup	ATP7A, CYSLTR1 +9 more	Duplication	not provided	GUncertain significance
Select item 1180551	GRCh37/hg19 Xp22.33-q28(chrX:60000-155234966)x1	KLHL34, KLHL4 +818 more	Copy number loss	not provided	GPathogenic
Select item 992648	GRCh37/hg19 Xp11.21-q28(chrX:56469080-155233731)x3	CPXCR1, GABRE +509 more	Copy number gain	not provided	GPathogenic
Select item 983156	GRCh37/hg19 Xp11.21-q28(chrX:55507789-155198481)x3	ARMCX4, CXorf51B +513 more	Copy number gain	See cases	GPathogenic
Select item 979829	GRCh37/hg19 Xq21.1-25(chrX:77514079-127770854)x1	ACSL4, ACTRT1 +201 more	Copy number loss	not provided	GPathogenic
Select item 816363	GRCh37/hg19 Xq21.1(chrX:77514079-78015580)x0	LPAR4, CYSLTR1 +1 more	Copy number loss	not provided	GUncertain significance
Select item 688137	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	ARHGAP36, ARHGAP4 +818 more	Copy number loss	not provided	GPathogenic
Select item 687519	GRCh37/hg19 Xp11.21-q28(chrX:54941868-155233731)x1	AWAT1, AWAT2 +524 more	Copy number loss	not provided	GUncertain significance
Select item 686630	GRCh37/hg19 Xq13.3-21.31(chrX:74667077-90312981)x1	APOOL, ATP7A +34 more	Copy number loss	not provided	GPathogenic
Select item 685566	GRCh37/hg19 Xp11.1-q28(chrX:58455352-155233731)x1	AWAT2, BCAP31 +502 more	Copy number loss	not provided	GPathogenic
Select item 685331	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4	BEX1, BEX2 +818 more	Copy number gain	not provided	GPathogenic
Select item 684962	GRCh37/hg19 Xp11.4-q21.32(chrX:40572613-92796528)x1	ABCB7, AKAP4 +281 more	Copy number loss	not provided	GPathogenic
Select item 626291	Single allele	AKAP14, CCDC22 +733 more	Duplication	Syndromic X-linked intellectual disability Lubs type	GPathogenic
Select item 564863	GRCh37/hg19 Xq21.1(chrX:77259796-77537309)x3	PGK1, CYSLTR1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 564862	GRCh37/hg19 Xq21.1(chrX:77259796-77537309)x2	PGK1, CYSLTR1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 564860	GRCh37/hg19 Xq21.1(chrX:76820808-78113526)x3	ATP7A, ATRX +8 more	Copy number gain	not provided	GLikely pathogenic
Select item 564772	GRCh37/hg19 Xp22.31-q21.31(chrX:7841947-90815333)x1,2	RPS6KA6, UPRT +413 more	Copy number gain	not provided	GPathogenic
Select item 545551	NC_000023.10:g.36649710_136649711del100000002insG	AMER1, AMMECR1 +541 more	Indel	Heterotaxy, visceral, 1, X-linked	GPathogenic
Select item 488014	Single allele	ARSF, CFAP47 +2632 more	Duplication	Autism +1 more	GPathogenic
Select item 487581	NC_000023.11:g.78195010_79012636del	RTL3, MIR4328 +7 more	Deletion	not provided	GPathogenic
Select item 443974	GRCh37/hg19 Xp22.33-q28(chrX:168547-155233731)	ABCB7, ABCD1 +818 more	Copy number gain	See cases	GPathogenic
Select item 443946	GRCh37/hg19 Xp22.33-q23(chrX:168547-112474026)x1	EIF1AX, EIF2S3 +539 more	Copy number loss	See cases	GPathogenic
Select item 443504	GRCh37/hg19 Xp21.2-q28(chrX:31088082-155233731)x1	PNMA5, PNMA6A +695 more	Copy number loss	See cases	GPathogenic
Select item 443017	GRCh37/hg19 Xp11.21-q28(chrX:56457791-155233731)x3	NAA10, NALF2 +509 more	Copy number gain	See cases	GPathogenic
Select item 442832	GRCh37/hg19 Xp21.1-q22.1(chrX:37521774-98488534)x1	ABCB7, AKAP4 +300 more	Copy number loss	See cases	GPathogenic
Select item 442751	GRCh37/hg19 Xq21.1(chrX:77212971-77537309)x3	ATP7A, CYSLTR1 +3 more	Copy number gain	See cases	GUncertain significance
Select item 442724	GRCh37/hg19 Xp22.33-q28(chrX:168547-151304063)x1	AP1S2, APEX2 +731 more	Copy number loss	See cases	GPathogenic
Select item 442646	GRCh37/hg19 Xp11.21-q28(chrX:57415659-155233731)x3	OR13H1, OTUD6A +505 more	Copy number gain	See cases	GPathogenic
Select item 442531	GRCh37/hg19 Xp11.21-q28(chrX:55000501-155230750)x3	ABCB7, ABCD1 +523 more	Copy number gain	See cases	GPathogenic
Select item 442321	GRCh37/hg19 Xp11.21-q28(chrX:57511767-155233731)x3	YIPF6, ZBTB33 +505 more	Copy number gain	See cases	GPathogenic
Select item 442018	GRCh37/hg19 Xp11.21-q21.1(chrX:55240087-78225374)x1	ABCB7, AMER1 +104 more	Copy number loss	See cases	GPathogenic
Select item 441843	GRCh37/hg19 Xq13.3-24(chrX:74560735-116609286)	PLP1, PLS3 +158 more	Copy number loss	See cases	GPathogenic
Select item 425520	GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2	BEX4, BEX5 +566 more	Copy number gain	not provided	GUncertain significance
Select item 395718	GRCh37/hg19 Xp22.33-q28(chrX:70297-155246585)x1	TMLHE, TMSB15A +819 more	Copy number loss	See cases	GPathogenic
Select item 395687	GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)	ABCB7, ABCD1 +819 more	Copy number loss	See cases	GPathogenic
Select item 395686	GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)x4	BEX1, BEX2 +819 more	Copy number gain	See cases	GPathogenic
Select item 394706	GRCh37/hg19 Xp22.33-q28(chrX:60701-155246225)x3	ABCB7, ABCD1 +819 more	Copy number gain	See cases	GPathogenic
Select item 394672	GRCh37/hg19 Xp22.33-q28(chrX:318707-155224707)x1	ABCB7, ADGRG2 +818 more	Copy number loss	See cases	GPathogenic
Select item 394066	GRCh37/hg19 Xq13.2-27.1(chrX:72224362-139262228)x4	TCEAL8, TCEAL9 +299 more	Copy number gain	See cases	GPathogenic
Select item 394013	GRCh37/hg19 Xp22.33-q28(chrX:71267-155255792)x1	ABCB7, ABCD1 +819 more	Copy number loss	See cases	GPathogenic
Select item 253652	GRCh37/hg19 Xp22.33-q28(chrX:71267-155246643)x3	ABCB7, ABCD1 +819 more	Copy number gain	See cases	GPathogenic
Select item 253624	GRCh37/hg19 Xp22.33-q28(chrX:60701-155246271)x3	TMEM255A, TMEM31 +819 more	Copy number gain	See cases	GPathogenic
Select item 253616	GRCh37/hg19 Xq11.1-28(chrX:62063537-155246643)x3	ABCB7, ABCD1 +503 more	Copy number gain	See cases	GPathogenic
Select item 253613	GRCh37/hg19 Xp22.2-q28(chrX:13147668-155250222)x3	ABCB7, ABCD1 +783 more	Copy number gain	See cases	GPathogenic
Select item 253602	GRCh37/hg19 Xp22.33-q28(chrX:176426-155236656)x3	ABCB7, ABCD1 +818 more	Copy number gain	See cases	GPathogenic
Select item 253583	GRCh37/hg19 Xp22.33-q28(chrX:225816-155234036)x2	PNMA3, PLP1 +818 more	Copy number gain	See cases	GPathogenic
Select item 253572	GRCh37/hg19 Xq11.1-28(chrX:62063537-155250222)x3	ABCB7, ABCD1 +503 more	Copy number gain	See cases	GPathogenic
Select item 253495	GRCh37/hg19 Xp22.33-q28(chrX:71267-155224766)x1	MAGEB4, MAGEB5 +818 more	Copy number loss	See cases	GPathogenic
Select item 253492	GRCh37/hg19 Xp22.33-q28(chrX:71267-155255839)x1	ABCB7, ABCD1 +819 more	Copy number loss	See cases	GPathogenic
Select item 253487	GRCh37/hg19 Xp22.33-q28(chrX:2707626-155250222)x2	RPS6KA3, RPS6KA6 +819 more	Copy number gain	See cases	GPathogenic
Select item 253458	GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x2	ABCB7, ABCD1 +818 more	Copy number gain	See cases	GPathogenic
Select item 253438	GRCh37/hg19 Xp22.33-q28(chrX:176426-155250222)x3	RRAGB, RS1 +819 more	Copy number gain	See cases	GPathogenic
Select item 253436	GRCh37/hg19 Xp11.3-q21.1(chrX:44734936-79676121)x3	ABCB7, AKAP4 +250 more	Copy number gain	See cases	GPathogenic
Select item 253432	GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x3	ARL13A, ARMCX1 +818 more	Copy number gain	See cases	GPathogenic
Select item 253389	GRCh37/hg19 Xp22.33-q28(chrX:71267-155234036)x2	HDAC6, HTATSF1 +818 more	Copy number gain	See cases	GPathogenic
Select item 253376	GRCh37/hg19 Xp22.33-q28(chrX:70297-155255839)x3	ABCB7, ABCD1 +819 more	Copy number gain	See cases	GPathogenic
Select item 161649	NM_006639.4(CYSLTR1):c.68del (p.Asn23fs)	CYSLTR1 (N23fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance

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