ClinVar for Gene (Select 80731) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3326024	NM_001316349.2(THSD7B):c.3101G>T (p.Gly1034Val)	THSD7B (G1034V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326023	NM_001316349.2(THSD7B):c.140-65504G>C	THSD7B	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3326022	NM_001316349.2(THSD7B):c.4574T>C (p.Leu1525Pro)	THSD7B (L1525P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326021	NM_001316349.2(THSD7B):c.4557A>T (p.Lys1519Asn)	THSD7B (K1519N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326020	NM_001316349.2(THSD7B):c.4801G>A (p.Asp1601Asn)	THSD7B (D1601N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326019	NM_001316349.2(THSD7B):c.2566G>A (p.Gly856Ser)	THSD7B (G856S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326018	NM_001316349.2(THSD7B):c.2987C>T (p.Pro996Leu)	THSD7B (P996L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326017	NM_001316349.2(THSD7B):c.4033G>A (p.Glu1345Lys)	THSD7B (E1345K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326016	NM_001316349.2(THSD7B):c.1352C>T (p.Ala451Val)	THSD7B (A451V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326015	NM_001316349.2(THSD7B):c.3850C>T (p.Arg1284Trp)	THSD7B (R1284W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326014	NM_001316349.2(THSD7B):c.325T>G (p.Ser109Ala)	THSD7B (S109A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326013	NM_001316349.2(THSD7B):c.362G>A (p.Arg121His)	THSD7B (R121H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3326011	NM_001316349.2(THSD7B):c.1958G>A (p.Arg653His)	THSD7B (R653H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326010	NM_001316349.2(THSD7B):c.832A>G (p.Thr278Ala)	THSD7B (T278A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326009	NM_001316349.2(THSD7B):c.2198C>T (p.Pro733Leu)	THSD7B (P733L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177249	NM_001316349.2(THSD7B):c.1048A>G (p.Lys350Glu)	THSD7B (K350E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177248	NM_001316349.2(THSD7B):c.175G>A (p.Gly59Arg)	THSD7B (G59R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177247	NM_001316349.2(THSD7B):c.869C>T (p.Ser290Leu)	THSD7B (S290L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177246	NM_001316349.2(THSD7B):c.4495A>G (p.Ile1499Val)	THSD7B (I1499V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177245	NM_001316349.2(THSD7B):c.4411C>T (p.Arg1471Trp)	THSD7B (R1471W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177244	NM_001316349.2(THSD7B):c.4189C>T (p.Arg1397Cys)	THSD7B (R1397C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177243	NM_001316349.2(THSD7B):c.4022C>A (p.Ala1341Asp)	THSD7B (A1341D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177242	NM_001316349.2(THSD7B):c.3671A>G (p.Gln1224Arg)	THSD7B (Q1224R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177241	NM_001316349.2(THSD7B):c.3595G>A (p.Ala1199Thr)	THSD7B (A1199T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177240	NM_001316349.2(THSD7B):c.3563C>T (p.Thr1188Ile)	THSD7B (T1188I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177238	NM_001316349.2(THSD7B):c.3457C>T (p.Arg1153Cys)	THSD7B (R1153C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177236	NM_001316349.2(THSD7B):c.2851C>T (p.Arg951Trp)	THSD7B (R951W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177235	NM_001316349.2(THSD7B):c.364G>A (p.Gly122Ser)	THSD7B (G122S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177234	NM_001316349.2(THSD7B):c.2770G>A (p.Asp924Asn)	THSD7B (D924N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177233	NM_001316349.2(THSD7B):c.2768G>C (p.Cys923Ser)	THSD7B (C923S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177232	NM_001316349.2(THSD7B):c.2642C>T (p.Thr881Met)	THSD7B (T881M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177231	NM_001316349.2(THSD7B):c.2486G>A (p.Gly829Glu)	THSD7B (G829E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177230	NM_001316349.2(THSD7B):c.2358G>C (p.Glu786Asp)	THSD7B (E786D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177229	NM_001316349.2(THSD7B):c.2131G>A (p.Gly711Arg)	THSD7B (G711R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177228	NM_001316349.2(THSD7B):c.2128G>T (p.Val710Leu)	THSD7B (V710L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177227	NM_001316349.2(THSD7B):c.1945C>T (p.Leu649Phe)	THSD7B (L649F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177226	NM_001316349.2(THSD7B):c.1930C>A (p.Pro644Thr)	THSD7B (P644T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177223	NM_001316349.2(THSD7B):c.1408G>A (p.Ala470Thr)	THSD7B (A470T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177222	NM_001316349.2(THSD7B):c.211G>T (p.Val71Phe)	THSD7B (V71F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177221	NM_001316349.2(THSD7B):c.1280C>T (p.Thr427Met)	THSD7B (T427M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177220	NM_001316349.2(THSD7B):c.1175G>A (p.Gly392Glu)	THSD7B (G392E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177219	NM_001316349.2(THSD7B):c.1121G>C (p.Gly374Ala)	THSD7B (G374A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177218	NM_001316349.2(THSD7B):c.1096C>T (p.Arg366Trp)	THSD7B (R366W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062608	GRCh37/hg19 2q21.2-23.2(chr2:134589311-149951291)x3	ACMSD, ACVR2A +26 more	Copy number gain	not specified	GLikely pathogenic
Select item 2685863	GRCh37/hg19 2q22.1(chr2:137489170-137751231)x3	THSD7B	Copy number gain	not provided	GUncertain significance
Select item 2684731	GRCh37/hg19 2q22.1(chr2:138388665-138461937)x1	THSD7B	Copy number loss	not provided	GUncertain significance
Select item 2620896	NM_001316349.2(THSD7B):c.2092A>G (p.Ile698Val)	THSD7B (I698V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620667	NM_001316349.2(THSD7B):c.3622C>T (p.Arg1208Cys)	THSD7B (R1208C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618665	NM_001316349.2(THSD7B):c.322G>A (p.Val108Ile)	THSD7B (V108I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617852	NM_001316349.2(THSD7B):c.3851G>A (p.Arg1284Gln)	THSD7B (R1284Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608379	NM_001316349.2(THSD7B):c.3999C>G (p.His1333Gln)	THSD7B (H1333Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601793	NM_001316349.2(THSD7B):c.3293G>A (p.Gly1098Asp)	THSD7B (G1098D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597981	NM_001316349.2(THSD7B):c.3029G>A (p.Gly1010Glu)	THSD7B (G1010E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593229	NM_001316349.2(THSD7B):c.3167A>G (p.Glu1056Gly)	THSD7B (E1056G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588517	NM_001316349.2(THSD7B):c.3558T>A (p.Asn1186Lys)	THSD7B (N1186K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559466	NM_001316349.2(THSD7B):c.2657A>G (p.Asn886Ser)	THSD7B (N886S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553728	NM_001316349.2(THSD7B):c.2843G>T (p.Arg948Leu)	THSD7B (R948L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541987	NM_001316349.2(THSD7B):c.1448C>T (p.Thr483Met)	THSD7B (T483M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541691	NM_001316349.2(THSD7B):c.4358A>C (p.Asp1453Ala)	THSD7B (D1453A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541067	NM_001316349.2(THSD7B):c.3947G>A (p.Gly1316Asp)	THSD7B (G1316D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536386	NM_001316349.2(THSD7B):c.1543C>T (p.Arg515Cys)	THSD7B (R515C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524487	NM_001316349.2(THSD7B):c.1919G>A (p.Gly640Glu)	THSD7B (G640E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521108	NM_001316349.2(THSD7B):c.3590A>C (p.Glu1197Ala)	THSD7B (E1197A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496575	NM_001316349.2(THSD7B):c.1867G>A (p.Asp623Asn)	THSD7B (D623N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490995	NM_001316349.2(THSD7B):c.3095A>G (p.Tyr1032Cys)	THSD7B (Y1032C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483813	NM_001316349.2(THSD7B):c.1931C>A (p.Pro644His)	THSD7B (P644H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480607	NM_001316349.2(THSD7B):c.2177C>T (p.Thr726Ile)	THSD7B (T726I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471635	NM_001316349.2(THSD7B):c.389A>G (p.Glu130Gly)	THSD7B (E130G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411402	NM_001316349.2(THSD7B):c.860A>G (p.His287Arg)	THSD7B (H287R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407770	NM_001316349.2(THSD7B):c.4702A>T (p.Ile1568Phe)	THSD7B (I1568F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396086	NM_001316349.2(THSD7B):c.1594G>A (p.Val532Met)	THSD7B (V532M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393889	NM_001316349.2(THSD7B):c.140-65491A>G	THSD7B	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 2392275	NM_001316349.2(THSD7B):c.1433A>T (p.Asn478Ile)	THSD7B (N478I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377471	NM_001316349.2(THSD7B):c.1705G>A (p.Val569Ile)	THSD7B (V569I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369315	NM_001316349.2(THSD7B):c.1132G>A (p.Glu378Lys)	THSD7B (E378K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355967	NM_001316349.2(THSD7B):c.3733G>A (p.Val1245Met)	THSD7B (V1245M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355459	NM_001316349.2(THSD7B):c.1160C>A (p.Ala387Asp)	THSD7B (A387D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346712	NM_001316349.2(THSD7B):c.3632G>A (p.Ser1211Asn)	THSD7B (S1211N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343512	NM_001316349.2(THSD7B):c.1823C>T (p.Thr608Met)	THSD7B (T608M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335313	NM_001316349.2(THSD7B):c.4702A>G (p.Ile1568Val)	THSD7B (I1568V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325352	NM_001316349.2(THSD7B):c.2891G>A (p.Arg964His)	THSD7B (R964H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315235	NM_001316349.2(THSD7B):c.538T>A (p.Cys180Ser)	THSD7B (C180S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314071	NM_001316349.2(THSD7B):c.376C>G (p.Pro126Ala)	THSD7B (P126A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312108	NM_001316349.2(THSD7B):c.1798A>T (p.Met600Leu)	THSD7B (M600L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298202	NM_001316349.2(THSD7B):c.3613G>A (p.Val1205Ile)	THSD7B (V1205I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296553	NM_001316349.2(THSD7B):c.4325A>G (p.Asn1442Ser)	THSD7B (N1442S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285988	NM_001316349.2(THSD7B):c.4718T>C (p.Ile1573Thr)	THSD7B (I1573T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274985	NM_001316349.2(THSD7B):c.3812G>A (p.Arg1271Gln)	THSD7B (R1271Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271646	NM_001316349.2(THSD7B):c.4363G>A (p.Val1455Ile)	THSD7B (V1455I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2270512	NM_001316349.2(THSD7B):c.2183G>A (p.Arg728His)	THSD7B (R728H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266941	NM_001316349.2(THSD7B):c.1715A>G (p.Asn572Ser)	THSD7B (N572S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241023	NM_001316349.2(THSD7B):c.2747T>C (p.Val916Ala)	THSD7B (V916A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237930	NM_001316349.2(THSD7B):c.3238C>T (p.Arg1080Cys)	THSD7B (R1080C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229320	NM_001316349.2(THSD7B):c.3433C>A (p.Pro1145Thr)	THSD7B (P1145T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228932	NM_001316349.2(THSD7B):c.2877T>G (p.Cys959Trp)	THSD7B (C959W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228279	NM_001316349.2(THSD7B):c.3557A>C (p.Asn1186Thr)	THSD7B (N1186T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207520	NM_001316349.2(THSD7B):c.4301C>T (p.Thr1434Ile)	THSD7B (T1434I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808691	GRCh37/hg19 2q22.1(chr2:138298575-138390341)x1	THSD7B	Copy number loss	not provided	GUncertain significance
Select item 1703543	GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	ABCA12, ABCB11 +1216 more	Copy number gain	Mosaic trisomy 2	GPathogenic
Select item 1679114	GRCh37/hg19 2q13-22.3(chr2:112475655-145691999)x3	EPB41L5, ERCC3 +120 more	Copy number gain	2q13q22.3 microduplication syndrome	GPathogenic

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