ClinVar for Gene (Select 84889) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3165562	NM_032803.6(SLC7A3):c.977T>G (p.Leu326Arg)	SLC7A3 (L326R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165560	NM_032803.6(SLC7A3):c.613A>G (p.Met205Val)	SLC7A3 (M205V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165559	NM_032803.6(SLC7A3):c.608T>C (p.Phe203Ser)	SLC7A3 (F203S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165558	NM_032803.6(SLC7A3):c.362A>G (p.Tyr121Cys)	SLC7A3 (Y121C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165557	NM_032803.6(SLC7A3):c.1534G>A (p.Val512Met)	SLC7A3 (V512M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165556	NM_032803.6(SLC7A3):c.1132A>G (p.Thr378Ala)	SLC7A3 (T378A)	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 3058308	NM_032803.6(SLC7A3):c.216G>A (p.Val72=)	SLC7A3	Single nucleotide variant (synonymous variant)	SLC7A3-related condition	GLikely benign
Select item 3051275	NM_032803.6(SLC7A3):c.852C>T (p.Ile284=)	SLC7A3	Single nucleotide variant (synonymous variant)	SLC7A3-related condition	GLikely benign
Select item 3046573	NM_032803.6(SLC7A3):c.357C>T (p.Leu119=)	SLC7A3	Single nucleotide variant (synonymous variant)	SLC7A3-related condition	GLikely benign
Select item 3040510	NM_032803.6(SLC7A3):c.1005T>C (p.Tyr335=)	SLC7A3	Single nucleotide variant (synonymous variant)	SLC7A3-related condition	GBenign
Select item 3024654	GRCh37/hg19 Xq12-28(chrX:67292994-155240074)x3	TMEM31, TMEM35A +488 more	Copy number gain	not provided	GPathogenic
Select item 2663780	NC_000023.11:g.(?_66445907)_(78172208_?)dup	KIF4A, LOC130068402 +206 more	Duplication	Xq13q21 duplication	GPathogenic
Select item 2660836	NM_032803.6(SLC7A3):c.618C>T (p.Ile206=)	SLC7A3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660835	NM_032803.6(SLC7A3):c.1746C>T (p.Phe582=)	SLC7A3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660834	NM_032803.6(SLC7A3):c.1761G>A (p.Gln587=)	SLC7A3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660833	NM_032803.6(SLC7A3):c.1791A>G (p.Gln597=)	SLC7A3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2630960	NM_032803.6(SLC7A3):c.147C>T (p.Gly49=)	SLC7A3	Single nucleotide variant (synonymous variant)	SLC7A3-related condition	GUncertain significance
Select item 2630406	NM_032803.6(SLC7A3):c.643C>T (p.His215Tyr)	SLC7A3 (H215Y)	Single nucleotide variant (missense variant)	SLC7A3-related condition	GUncertain significance
Select item 2628964	NM_032803.6(SLC7A3):c.1571T>C (p.Ile524Thr)	SLC7A3 (I524T)	Single nucleotide variant (missense variant)	SLC7A3-related condition	GUncertain significance
Select item 2616020	NM_032803.6(SLC7A3):c.80G>A (p.Arg27His)	SLC7A3 (R27H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605705	NM_032803.6(SLC7A3):c.67A>G (p.Met23Val)	SLC7A3 (M23V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600942	NM_032803.6(SLC7A3):c.575T>C (p.Val192Ala)	SLC7A3 (V192A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598910	NM_032803.6(SLC7A3):c.1703C>T (p.Ala568Val)	SLC7A3 (A568V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545577	NM_032803.6(SLC7A3):c.472C>G (p.His158Asp)	SLC7A3 (H158D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2506546	GRCh37/hg19 Xp22.33-q28(chrX:200855-155240074)	BMX, CXorf38 +821 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 2425299	NC_000023.10:g.(?_69748945)_(70644108_?)dup	CXorf65, FOXO4 +11 more	Duplication	FG syndrome 1	GUncertain significance
Select item 2399746	NM_032803.6(SLC7A3):c.1235T>C (p.Ile412Thr)	SLC7A3 (I412T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379772	NM_032803.6(SLC7A3):c.1001G>A (p.Arg334His)	SLC7A3 (R334H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361766	NM_032803.6(SLC7A3):c.1798C>T (p.Arg600Cys)	SLC7A3 (R600C)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2353203	NM_032803.6(SLC7A3):c.845G>A (p.Arg282His)	SLC7A3 (R282H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2324392	NM_032803.6(SLC7A3):c.715C>T (p.Pro239Ser)	SLC7A3 (P239S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244069	NM_032803.6(SLC7A3):c.434C>T (p.Ser145Phe)	SLC7A3 (S145F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241215	NM_032803.6(SLC7A3):c.277C>T (p.Arg93Cys)	SLC7A3 (R93C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216704	NM_032803.6(SLC7A3):c.461T>C (p.Leu154Pro)	SLC7A3 (L154P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1707442	GRCh37/hg19 Xp22.2-q28(chrX:11522765-155233731)x1	MIR224, MIR424 +793 more	Copy number loss	See cases	GPathogenic
Select item 1704345	GRCh37/hg19 Xp22.33-q28(chrX:61545-155226048)x2	CT55, CT83 +821 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 1703584	GRCh37/hg19 Xq11.1-28(chrX:62685885-155233731)	H2AB3, H2BW1 +502 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703580	GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	ABCB7, ABCD1 +822 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703579	GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	SCML2, SEPTIN6 +822 more	Copy number gain	Hypotonia +2 more	GPathogenic
Select item 1526804	GRCh37/hg19 Xq11.1-21.1(chrX:61974855-79123671)	ABCB7, AMER1 +92 more	Copy number gain	not specified	GPathogenic
Select item 1526803	GRCh37/hg19 Xq11.1-21.1(chrX:61877278-79123671)	ABCB7, AMER1 +92 more	Copy number gain	not specified	GPathogenic
Select item 1341233	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	CXorf51B, GAGE12H +821 more	Copy number loss	not provided	GPathogenic
Select item 1341223	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3	ABCB7, ABCD1 +821 more	Copy number gain	not provided	GPathogenic
Select item 1340039	GRCh37/hg19 Xq13.1(chrX:69917640-70638292)x2	CXorf65, FOXO4 +11 more	Copy number gain	not provided	GUncertain significance
Select item 1180551	GRCh37/hg19 Xp22.33-q28(chrX:60000-155234966)x1	CXorf49B, CXorf51A +821 more	Copy number loss	not provided	GPathogenic
Select item 992648	GRCh37/hg19 Xp11.21-q28(chrX:56469080-155233731)x3	ABCB7, ABCD1 +510 more	Copy number gain	not provided	GPathogenic
Select item 989433	Single allele	DLG3, GDPD2 +3 more	Duplication	Intellectual disability	GUncertain significance
Select item 983156	GRCh37/hg19 Xp11.21-q28(chrX:55507789-155198481)x3	ABCB7, ABCD1 +514 more	Copy number gain	See cases	GPathogenic
Select item 807746	NM_032803.6(SLC7A3):c.1011G>C (p.Val337=)	SLC7A3	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 807745	NM_032803.6(SLC7A3):c.1766G>C (p.Ser589Thr)	SLC7A3 (S589T)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 694513	46,Y,inv(X)(p21.1q13.3)	ABCB7, AKAP4 +270 more	Inversion	Elevated circulating creatine kinase concentration	GLikely pathogenic
Select item 688137	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	RBMXL3, RENBP +821 more	Copy number loss	not provided	GPathogenic
Select item 687519	GRCh37/hg19 Xp11.21-q28(chrX:54941868-155233731)x1	RBMX2, RBMXL3 +525 more	Copy number loss	not provided	GUncertain significance
Select item 685566	GRCh37/hg19 Xp11.1-q28(chrX:58455352-155233731)x1	AMOT, APLN +503 more	Copy number loss	not provided	GPathogenic
Select item 685331	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4	ZNF275, ZNF280C +821 more	Copy number gain	not provided	GPathogenic
Select item 684962	GRCh37/hg19 Xp11.4-q21.32(chrX:40572613-92796528)x1	ITGB1BP2, RGN +281 more	Copy number loss	not provided	GPathogenic
Select item 626291	Single allele	PAGE2B, PAGE3 +733 more	Duplication	Syndromic X-linked intellectual disability Lubs type	GPathogenic
Select item 564772	GRCh37/hg19 Xp22.31-q21.31(chrX:7841947-90815333)x1,2	ABCB7, ACE2 +415 more	Copy number gain	not provided	GPathogenic
Select item 545551	NC_000023.10:g.36649710_136649711del100000002insG	ADGRG4, ACTRT1 +541 more	Indel	Heterotaxy, visceral, 1, X-linked	GPathogenic
Select item 488014	Single allele	ARMCX3, CT47A11 +2631 more	Duplication	Autism +1 more	GPathogenic
Select item 443974	GRCh37/hg19 Xp22.33-q28(chrX:168547-155233731)	TBL1X, TBX22 +818 more	Copy number gain	See cases	GPathogenic
Select item 443946	GRCh37/hg19 Xp22.33-q23(chrX:168547-112474026)x1	ABCB7, ACE2 +539 more	Copy number loss	See cases	GPathogenic
Select item 443504	GRCh37/hg19 Xp21.2-q28(chrX:31088082-155233731)x1	ABCB7, ABCD1 +695 more	Copy number loss	See cases	GPathogenic
Select item 443017	GRCh37/hg19 Xp11.21-q28(chrX:56457791-155233731)x3	RBMX2, RBMXL3 +509 more	Copy number gain	See cases	GPathogenic
Select item 442832	GRCh37/hg19 Xp21.1-q22.1(chrX:37521774-98488534)x1	PPP1R3F, RGN +300 more	Copy number loss	See cases	GPathogenic
Select item 442724	GRCh37/hg19 Xp22.33-q28(chrX:168547-151304063)x1	HDAC8, HDX +731 more	Copy number loss	See cases	GPathogenic
Select item 442646	GRCh37/hg19 Xp11.21-q28(chrX:57415659-155233731)x3	LHFPL1, LONRF3 +505 more	Copy number gain	See cases	GPathogenic
Select item 442531	GRCh37/hg19 Xp11.21-q28(chrX:55000501-155230750)x3	MECP2, MED12 +523 more	Copy number gain	See cases	GPathogenic
Select item 442354	GRCh37/hg19 Xp22.33-q13.3(chrX:168546-74549686)	GAGE1, GAGE12H +390 more	Copy number loss	See cases	GPathogenic
Select item 442321	GRCh37/hg19 Xp11.21-q28(chrX:57511767-155233731)x3	ABCB7, ABCD1 +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 425520	GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2	AWAT2, BCLAF3 +568 more	Copy number gain	not provided	GUncertain significance
Select item 395718	GRCh37/hg19 Xp22.33-q28(chrX:70297-155246585)x1	FAM133A, FAM156A +819 more	Copy number loss	See cases	GPathogenic
Select item 395687	GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)	FOXO4, FOXP3 +819 more	Copy number loss	See cases	GPathogenic
Select item 395686	GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)x4	TMSB4X, TNMD +819 more	Copy number gain	See cases	GPathogenic
Select item 394706	GRCh37/hg19 Xp22.33-q28(chrX:60701-155246225)x3	GPKOW, PIN4 +819 more	Copy number gain	See cases	GPathogenic
Select item 394672	GRCh37/hg19 Xp22.33-q28(chrX:318707-155224707)x1	CT47A11, CT47A12 +818 more	Copy number loss	See cases	GPathogenic
Select item 394013	GRCh37/hg19 Xp22.33-q28(chrX:71267-155255792)x1	CT45A2, PIN4 +819 more	Copy number loss	See cases	GPathogenic
Select item 253652	GRCh37/hg19 Xp22.33-q28(chrX:71267-155246643)x3	ABCB7, ABCD1 +822 more	Copy number gain	See cases	GPathogenic
Select item 253624	GRCh37/hg19 Xp22.33-q28(chrX:60701-155246271)x3	GAGE12F, GAGE12G +822 more	Copy number gain	See cases	GPathogenic
Select item 253616	GRCh37/hg19 Xq11.1-28(chrX:62063537-155246643)x3	ABCB7, ABCD1 +504 more	Copy number gain	See cases	GPathogenic
Select item 253613	GRCh37/hg19 Xp22.2-q28(chrX:13147668-155250222)x3	FOXP3, FOXR2 +786 more	Copy number gain	See cases	GPathogenic
Select item 253602	GRCh37/hg19 Xp22.33-q28(chrX:176426-155236656)x3	MCTS1, MECP2 +821 more	Copy number gain	See cases	GPathogenic
Select item 253583	GRCh37/hg19 Xp22.33-q28(chrX:225816-155234036)x2	ABCB7, ABCD1 +821 more	Copy number gain	See cases	GPathogenic
Select item 253572	GRCh37/hg19 Xq11.1-28(chrX:62063537-155250222)x3	ABCB7, ABCD1 +504 more	Copy number gain	See cases	GPathogenic
Select item 253495	GRCh37/hg19 Xp22.33-q28(chrX:71267-155224766)x1	ABCB7, ABCD1 +821 more	Copy number loss	See cases	GPathogenic
Select item 253492	GRCh37/hg19 Xp22.33-q28(chrX:71267-155255839)x1	EOLA2, ERAS +822 more	Copy number loss	See cases	GPathogenic
Select item 253487	GRCh37/hg19 Xp22.33-q28(chrX:2707626-155250222)x2	ABCB7, ABCD1 +822 more	Copy number gain	See cases	GPathogenic
Select item 253458	GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x2	RENBP, REPS2 +821 more	Copy number gain	See cases	GPathogenic
Select item 253438	GRCh37/hg19 Xp22.33-q28(chrX:176426-155250222)x3	SPANXD, TCEAL4 +822 more	Copy number gain	See cases	GPathogenic
Select item 253436	GRCh37/hg19 Xp11.3-q21.1(chrX:44734936-79676121)x3	ALAS2, AMER1 +250 more	Copy number gain	See cases	GPathogenic
Select item 253432	GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x3	ARMCX2, CFAP47 +821 more	Copy number gain	See cases	GPathogenic
Select item 253389	GRCh37/hg19 Xp22.33-q28(chrX:71267-155234036)x2	ABCB7, ABCD1 +821 more	Copy number gain	See cases	GPathogenic
Select item 253376	GRCh37/hg19 Xp22.33-q28(chrX:70297-155255839)x3	MAGEE2, MTRNR2L10 +822 more	Copy number gain	See cases	GPathogenic
Select item 161091	GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3	LOC116309160, LOC116309161 +2631 more	Copy number gain	See cases	GPathogenic
Select item 161089	GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1	LOC130068156, LOC130068157 +2632 more	Copy number loss	See cases	GPathogenic
Select item 161088	GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1	ABCB7, ABCD1 +2631 more	Copy number loss	See cases	GPathogenic
Select item 160983	GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1	ABCB7, ABCD1 +2632 more	Copy number loss	See cases	GPathogenic

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