ClinVar for Gene (Select 360200) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3179994	NM_001395513.1(TMPRSS9):c.1051A>G (p.Thr351Ala)	TMPRSS9 (T119A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179992	NM_001395513.1(TMPRSS9):c.1033G>A (p.Val345Met)	TMPRSS9 (V345M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179991	NM_001395513.1(TMPRSS9):c.1024A>G (p.Ile342Val)	TMPRSS9 (I342V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3179990	NM_001395513.1(TMPRSS9):c.83C>G (p.Ala28Gly)	TMPRSS9 (A28G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179989	NM_001395513.1(TMPRSS9):c.3253G>A (p.Gly1085Ser)	TIMM13, TMPRSS9 (G1051S +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3179987	NM_001395513.1(TMPRSS9):c.3199G>A (p.Gly1067Ser)	TIMM13, TMPRSS9 (G1033S +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3179986	NM_001395513.1(TMPRSS9):c.3176C>G (p.Thr1059Ser)	TIMM13, TMPRSS9 (T1025S +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3179985	NM_001395513.1(TMPRSS9):c.3153G>C (p.Glu1051Asp)	TIMM13, TMPRSS9 (E1051D +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3179984	NM_001395513.1(TMPRSS9):c.2974C>G (p.Arg992Gly)	TMPRSS9 (R958G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179983	NM_001395513.1(TMPRSS9):c.2833A>G (p.Thr945Ala)	TMPRSS9 (T713A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179982	NM_001395513.1(TMPRSS9):c.2822A>G (p.Tyr941Cys)	TMPRSS9 (Y709C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179981	NM_001395513.1(TMPRSS9):c.2789A>T (p.Glu930Val)	TMPRSS9 (E698V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179980	NM_001395513.1(TMPRSS9):c.2774C>G (p.Ala925Gly)	TMPRSS9 (A925G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179979	NM_001395513.1(TMPRSS9):c.2773G>A (p.Ala925Thr)	TMPRSS9 (A925T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179978	NM_001395513.1(TMPRSS9):c.2363C>T (p.Thr788Ile)	TMPRSS9 (T754I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179977	NM_001395513.1(TMPRSS9):c.2332C>T (p.Pro778Ser)	TMPRSS9 (P778S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179976	NM_001395513.1(TMPRSS9):c.2195G>T (p.Gly732Val)	TMPRSS9 (G500V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179975	NM_001395513.1(TMPRSS9):c.2184G>C (p.Glu728Asp)	TMPRSS9 (E728D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179974	NM_001395513.1(TMPRSS9):c.2143G>T (p.Asp715Tyr)	TMPRSS9 (D681Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179973	NM_001395513.1(TMPRSS9):c.2115C>G (p.Ile705Met)	TMPRSS9 (I671M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179972	NM_001395513.1(TMPRSS9):c.2108G>A (p.Arg703His)	TMPRSS9 (R471H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179971	NM_001395513.1(TMPRSS9):c.1924A>G (p.Ile642Val)	TMPRSS9 (I410V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3179969	NM_001395513.1(TMPRSS9):c.1787C>T (p.Ser596Phe)	TMPRSS9 (S596F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179968	NM_001395513.1(TMPRSS9):c.1493C>A (p.Pro498His)	TMPRSS9 (P266H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179967	NM_001395513.1(TMPRSS9):c.1370G>A (p.Arg457Gln)	TMPRSS9 (R423Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179966	NM_001395513.1(TMPRSS9):c.1131G>C (p.Glu377Asp)	TMPRSS9 (E343D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684882	GRCh37/hg19 19p13.3-13.2(chr19:260912-7246777)x3	UBXN6, UHRF1 +202 more	Copy number gain	not provided	GPathogenic
Select item 2648975	NM_001395513.1(TMPRSS9):c.3044G>A (p.Arg1015His)	TMPRSS9 (R1015H +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2648974	NM_001395513.1(TMPRSS9):c.2043G>A (p.Lys681=)	TMPRSS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648973	NM_001395513.1(TMPRSS9):c.1758G>A (p.Glu586=)	TMPRSS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648972	NM_001395513.1(TMPRSS9):c.747G>A (p.Pro249=)	TMPRSS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648971	NM_001395513.1(TMPRSS9):c.662C>T (p.Ala221Val)	TMPRSS9 (A187V +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2648970	NM_001395513.1(TMPRSS9):c.48G>C (p.Lys16Asn)	TMPRSS9 (K16N)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2622280	NM_001395513.1(TMPRSS9):c.925G>C (p.Val309Leu)	TMPRSS9 (V275L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602764	NM_001395513.1(TMPRSS9):c.245C>T (p.Thr82Met)	TMPRSS9 (T82M)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2602222	NM_001395513.1(TMPRSS9):c.1537G>A (p.Val513Met)	TMPRSS9 (V479M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594939	NM_001395513.1(TMPRSS9):c.218G>A (p.Arg73Gln)	TMPRSS9 (R73Q)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GLikely benign
Select item 2594263	NM_001395513.1(TMPRSS9):c.3272T>C (p.Ile1091Thr)	TIMM13, TMPRSS9 (I1057T +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2569571	NM_001395513.1(TMPRSS9):c.899C>T (p.Ser300Leu)	TMPRSS9 (S300L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569100	NM_001395513.1(TMPRSS9):c.437G>A (p.Arg146Gln)	TMPRSS9 (R146Q +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GLikely benign
Select item 2561477	NM_001395513.1(TMPRSS9):c.793G>A (p.Ala265Thr)	TMPRSS9 (A231T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2556739	NM_001395513.1(TMPRSS9):c.2951T>A (p.Val984Asp)	TMPRSS9 (V752D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556659	NM_001395513.1(TMPRSS9):c.2789A>C (p.Glu930Ala)	TMPRSS9 (E698A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554393	NM_001395513.1(TMPRSS9):c.2323C>T (p.Pro775Ser)	TMPRSS9 (P543S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549058	NM_001395513.1(TMPRSS9):c.3077T>C (p.Met1026Thr)	TMPRSS9 (M794T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549014	NM_001395513.1(TMPRSS9):c.1159C>G (p.Leu387Val)	TMPRSS9 (L155V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548387	NM_001395513.1(TMPRSS9):c.416T>A (p.Leu139Gln)	TMPRSS9 (L139Q +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2542327	NM_001395513.1(TMPRSS9):c.1026C>G (p.Ile342Met)	TMPRSS9 (I308M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520196	NM_001395513.1(TMPRSS9):c.1422G>A (p.Met474Ile)	TMPRSS9 (M242I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518736	NM_001395513.1(TMPRSS9):c.764G>C (p.Arg255Pro)	TMPRSS9 (R23P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516528	NM_001395513.1(TMPRSS9):c.2957C>T (p.Thr986Ile)	TMPRSS9 (T754I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516527	NM_001395513.1(TMPRSS9):c.2953A>G (p.Ile985Val)	TMPRSS9 (I753V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515755	NM_001395513.1(TMPRSS9):c.2003C>T (p.Thr668Met)	TMPRSS9 (T668M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2514191	NM_001395513.1(TMPRSS9):c.815T>C (p.Leu272Pro)	TMPRSS9 (L238P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507577	NM_001395513.1(TMPRSS9):c.1384C>T (p.Arg462Cys)	TMPRSS9 (R230C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494368	NM_001395513.1(TMPRSS9):c.446G>A (p.Arg149Gln)	TMPRSS9 (R115Q +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GLikely benign
Select item 2492978	NM_001395513.1(TMPRSS9):c.2933C>T (p.Pro978Leu)	TMPRSS9 (P746L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483904	NM_001395513.1(TMPRSS9):c.1693G>C (p.Ala565Pro)	TMPRSS9 (A333P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482038	NM_001395513.1(TMPRSS9):c.1079G>A (p.Cys360Tyr)	TMPRSS9 (C360Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479448	NM_001395513.1(TMPRSS9):c.1691G>T (p.Gly564Val)	TMPRSS9 (G332V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478614	NM_001395513.1(TMPRSS9):c.2386C>T (p.Leu796Phe)	TMPRSS9 (L762F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472290	NM_001395513.1(TMPRSS9):c.191G>A (p.Arg64Gln)	TMPRSS9 (R64Q)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2470080	NM_001395513.1(TMPRSS9):c.979G>A (p.Val327Met)	TMPRSS9 (V293M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461675	NM_001395513.1(TMPRSS9):c.2444C>T (p.Thr815Met)	TMPRSS9 (T583M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455664	NM_001395513.1(TMPRSS9):c.1916A>G (p.Asn639Ser)	TMPRSS9 (N407S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2445494	NC_000019.9:g.(?_1206913)_(3771740_?)dup	TCF3, PLK5 +80 more	Duplication	not provided	GUncertain significance
Select item 2427064	NC_000019.9:g.(?_1456055)_(2456931_?)dup	CSNK1G2, PEAK3 +35 more	Duplication	Lipodystrophy, partial, acquired, susceptibility to +1 more	GUncertain significance
Select item 2425228	NC_000019.9:g.(?_589946)_(5696788_?)dup	ABCA7, ABHD17A +151 more	Duplication	not provided	GUncertain significance
Select item 2423454	NC_000019.9:g.(?_589946)_(4818389_?)dup	ABCA7, ABHD17A +138 more	Duplication	not provided	GUncertain significance
Select item 2410799	NM_001395513.1(TMPRSS9):c.2336C>G (p.Pro779Arg)	TMPRSS9 (P547R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410164	NM_001395513.1(TMPRSS9):c.2110A>G (p.Met704Val)	TMPRSS9 (M472V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407760	NM_001395513.1(TMPRSS9):c.2878C>G (p.Arg960Gly)	TMPRSS9 (R926G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406705	NM_001395513.1(TMPRSS9):c.2375C>T (p.Thr792Met)	TMPRSS9 (T792M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400541	NM_001395513.1(TMPRSS9):c.1627G>A (p.Gly543Arg)	TMPRSS9 (G311R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396215	NM_001395513.1(TMPRSS9):c.1015G>A (p.Gly339Ser)	TMPRSS9 (G339S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394602	NM_001395513.1(TMPRSS9):c.857C>T (p.Thr286Met)	TMPRSS9 (T286M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385695	NM_001395513.1(TMPRSS9):c.2647C>T (p.Arg883Trp)	TMPRSS9 (R651W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384596	NM_001395513.1(TMPRSS9):c.1189G>A (p.Gly397Ser)	TMPRSS9 (G363S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382919	NM_001395513.1(TMPRSS9):c.1829G>A (p.Arg610Gln)	TMPRSS9 (R610Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378673	NM_001395513.1(TMPRSS9):c.2912C>T (p.Pro971Leu)	TMPRSS9 (P937L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366736	NM_001395513.1(TMPRSS9):c.560G>A (p.Arg187His)	TMPRSS9 (R153H +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2366512	NM_001395513.1(TMPRSS9):c.3215A>C (p.His1072Pro)	TIMM13, TMPRSS9 (H1038P +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2360590	NM_001395513.1(TMPRSS9):c.854C>T (p.Pro285Leu)	TMPRSS9 (P285L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359776	NM_001395513.1(TMPRSS9):c.2339C>T (p.Ser780Leu)	TMPRSS9 (S780L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359458	NM_001395513.1(TMPRSS9):c.433C>G (p.Gln145Glu)	TMPRSS9 (Q111E +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2359249	NM_001395513.1(TMPRSS9):c.3126C>G (p.Asp1042Glu)	TIMM13, TMPRSS9 (D1008E +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2357967	NM_001395513.1(TMPRSS9):c.1077G>T (p.Lys359Asn)	TMPRSS9 (K325N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355023	NM_001395513.1(TMPRSS9):c.1610G>A (p.Arg537Gln)	TMPRSS9 (R305Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354068	NM_001395513.1(TMPRSS9):c.1828C>T (p.Arg610Trp)	TMPRSS9 (R576W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353096	NM_001395513.1(TMPRSS9):c.763C>G (p.Arg255Gly)	TMPRSS9 (R221G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352005	NM_001395513.1(TMPRSS9):c.1355C>T (p.Pro452Leu)	TMPRSS9 (P220L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350961	NM_001395513.1(TMPRSS9):c.2570C>T (p.Ala857Val)	TMPRSS9 (A625V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347538	NM_001395513.1(TMPRSS9):c.2900C>A (p.Pro967His)	TMPRSS9 (P967H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347378	NM_001395513.1(TMPRSS9):c.199C>T (p.Arg67Trp)	TMPRSS9 (R67W)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2346131	NM_001395513.1(TMPRSS9):c.1219G>T (p.Ala407Ser)	TMPRSS9 (A175S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344628	NM_001395513.1(TMPRSS9):c.1181G>C (p.Ser394Thr)	TMPRSS9 (S162T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344343	NM_001395513.1(TMPRSS9):c.2048C>T (p.Ser683Phe)	TMPRSS9 (S649F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339451	NM_001395513.1(TMPRSS9):c.2107C>G (p.Arg703Gly)	TMPRSS9 (R471G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334909	NM_001395513.1(TMPRSS9):c.193G>A (p.Gly65Arg)	TMPRSS9 (G65R)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2327064	NM_001395513.1(TMPRSS9):c.2267C>T (p.Thr756Met)	TMPRSS9 (T756M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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