ClinVar for Gene (Select 7003) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 245

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3353968	NM_021961.6(TEAD1):c.402T>A (p.Thr134=)	TEAD1	Single nucleotide variant (synonymous variant)	TEAD1-related disorder	GLikely benign
Select item 3244784	NC_000011.9:g.(?_12883777)_(12886467_?)del	TEAD1	Deletion	not provided	GUncertain significance
Select item 3175565	NM_021961.6(TEAD1):c.932A>G (p.Gln311Arg)	TEAD1 (Q311R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3175564	NM_021961.6(TEAD1):c.734C>T (p.Ala245Val)	TEAD1 (A245V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3175563	NM_021961.6(TEAD1):c.53G>A (p.Arg18Lys)	TEAD1 (R18K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3175562	NM_021961.6(TEAD1):c.455G>A (p.Gly152Glu)	TEAD1 (G152E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3175561	NM_021961.6(TEAD1):c.1138A>G (p.Ser380Gly)	TEAD1 (S380G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3005745	NM_021961.6(TEAD1):c.1266G>A (p.Arg422=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004274	NM_021961.6(TEAD1):c.732T>C (p.His244=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3000323	NM_021961.6(TEAD1):c.908G>A (p.Gly303Glu)	TEAD1 (G303E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3000021	NM_021961.6(TEAD1):c.541C>T (p.Pro181Ser)	TEAD1 (P181S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2998523	NM_021961.6(TEAD1):c.1167+18_1167+19del	TEAD1	Deletion (intron variant)	not provided	GLikely benign
Select item 2996332	NM_021961.6(TEAD1):c.575-14G>A	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2994522	NM_021961.6(TEAD1):c.474G>A (p.Pro158=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2993762	NM_021961.6(TEAD1):c.589_591del (p.Ser197del)	TEAD1 (S197del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2992745	NM_021961.6(TEAD1):c.330+6C>T	LOC124421495, TEAD1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2985372	NM_021961.6(TEAD1):c.572C>G (p.Pro191Arg)	TEAD1 (P191R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2976009	NM_021961.6(TEAD1):c.391G>A (p.Val131Ile)	TEAD1 (V131I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2895231	NM_021961.6(TEAD1):c.390C>T (p.Ile130=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2893074	NM_021961.6(TEAD1):c.129T>C (p.Phe43=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2876115	NM_021961.6(TEAD1):c.591G>A (p.Ser197=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2874645	NM_021961.6(TEAD1):c.1254T>A (p.His418Gln)	TEAD1 (H418Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2868456	NM_021961.6(TEAD1):c.624T>C (p.Gly208=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2860974	NM_021961.6(TEAD1):c.902A>G (p.Asp301Gly)	TEAD1 (D301G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2854247	NM_021961.6(TEAD1):c.873+14T>C	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2848657	NM_021961.6(TEAD1):c.22G>C (p.Gly8Arg)	TEAD1 (G8R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2845843	NM_021961.6(TEAD1):c.1168-16T>C	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2812550	NM_021961.6(TEAD1):c.873+16C>A	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2810457	NM_021961.6(TEAD1):c.157T>C (p.Cys53Arg)	TEAD1 (C53R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2805700	NM_021961.6(TEAD1):c.1232A>G (p.Asn411Ser)	TEAD1 (N411S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2805366	NM_021961.6(TEAD1):c.1167+5T>C	TEAD1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2795587	NM_021961.6(TEAD1):c.699+18G>A	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2787583	NM_021961.6(TEAD1):c.723C>T (p.His241=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2781693	NM_021961.6(TEAD1):c.410A>G (p.His137Arg)	TEAD1 (H137R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2781330	NM_021961.6(TEAD1):c.268-11C>T	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2781098	NM_021961.6(TEAD1):c.1014+15G>T	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2769581	NM_021961.6(TEAD1):c.897A>G (p.Gln299=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2767250	NM_021961.6(TEAD1):c.268-4G>C	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2765863	NM_021961.6(TEAD1):c.512+19G>T	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2765195	NM_021961.6(TEAD1):c.1053C>T (p.Tyr351=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2761520	NM_021961.6(TEAD1):c.651C>T (p.Arg217=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2755679	NM_021961.6(TEAD1):c.1197T>C (p.Thr399=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2753595	NM_021961.6(TEAD1):c.310G>T (p.Asp104Tyr)	LOC124421495, TEAD1 (D104Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2721171	NM_021961.6(TEAD1):c.748A>G (p.Ser250Gly)	TEAD1 (S250G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2717627	NM_021961.6(TEAD1):c.1168-10del	TEAD1	Deletion (intron variant)	not provided	GLikely benign
Select item 2635459	NM_021961.6(TEAD1):c.699+5G>C	TEAD1	Single nucleotide variant (intron variant)	TEAD1-related disorder	GUncertain significance
Select item 2488884	NM_021961.6(TEAD1):c.562G>A (p.Ala188Thr)	TEAD1 (A188T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2478707	NM_021961.6(TEAD1):c.959T>C (p.Val320Ala)	TEAD1 (V320A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2419242	NM_021961.6(TEAD1):c.575-7C>G	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2418435	NM_021961.6(TEAD1):c.32G>A (p.Ser11Asn)	TEAD1 (S11N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2298674	NM_021961.6(TEAD1):c.1187C>T (p.Thr396Ile)	TEAD1 (T396I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2288427	NM_021961.6(TEAD1):c.428C>G (p.Pro143Arg)	TEAD1 (P143R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263932	NM_021961.6(TEAD1):c.1198C>G (p.Leu400Val)	TEAD1 (L400V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263863	NM_021961.6(TEAD1):c.1178A>G (p.Asn393Ser)	TEAD1 (N393S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2239202	NM_021961.6(TEAD1):c.681G>C (p.Gln227His)	TEAD1 (Q227H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2171495	NM_021961.6(TEAD1):c.369G>A (p.Ala123=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2154192	NM_021961.6(TEAD1):c.626G>A (p.Arg209His)	TEAD1 (R209H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2144747	NM_021961.6(TEAD1):c.717C>T (p.Phe239=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2132294	NM_021961.6(TEAD1):c.1170G>A (p.Val390=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2130022	NM_021961.6(TEAD1):c.1072A>G (p.Met358Val)	TEAD1 (M358V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2125122	NM_021961.6(TEAD1):c.721C>T (p.His241Tyr)	TEAD1 (H241Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2124648	NM_021961.6(TEAD1):c.137C>A (p.Ala46Asp)	TEAD1 (A46D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2124266	NM_021961.6(TEAD1):c.99G>A (p.Gly33=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2118906	NM_021961.6(TEAD1):c.832G>A (p.Gly278Arg)	TEAD1 (G278R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2118172	NM_021961.6(TEAD1):c.743C>A (p.Ser248Tyr)	TEAD1 (S248Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2106387	NM_021961.6(TEAD1):c.951T>C (p.Asn317=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2104814	NM_021961.6(TEAD1):c.407T>C (p.Ile136Thr)	TEAD1 (I136T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2102286	NM_021961.6(TEAD1):c.365T>C (p.Met122Thr)	TEAD1 (M122T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2094833	NM_021961.6(TEAD1):c.261A>C (p.Arg87Ser)	TEAD1 (R87S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2093943	NM_021961.6(TEAD1):c.604T>C (p.Ser202Pro)	TEAD1 (S202P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2091482	NM_021961.6(TEAD1):c.1167+18T>G	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2090757	NM_021961.6(TEAD1):c.718G>A (p.Val240Met)	TEAD1 (V240M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2084010	NM_021961.6(TEAD1):c.1150A>G (p.Asn384Asp)	TEAD1 (N384D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2083961	NM_021961.6(TEAD1):c.513-15TC[2]	TEAD1	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2083372	NM_021961.6(TEAD1):c.873+3_873+6del	TEAD1	Deletion (splice donor variant)	not provided	GUncertain significance
Select item 2079285	NM_021961.6(TEAD1):c.1050A>T (p.Val350=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2074263	NM_021961.6(TEAD1):c.439C>T (p.Arg147Cys)	TEAD1 (R147C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2065510	NM_021961.6(TEAD1):c.510A>G (p.Gln170=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2056717	NM_021961.6(TEAD1):c.874-20C>T	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2040561	NM_021961.6(TEAD1):c.268-5T>G	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2037601	NM_021961.6(TEAD1):c.1112A>G (p.His371Arg)	TEAD1 (H371R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2026880	NM_021961.6(TEAD1):c.203-10T>C	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2019574	NM_021961.6(TEAD1):c.512+9G>C	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2012351	NM_021961.6(TEAD1):c.1029G>A (p.Arg343=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2012291	NM_021961.6(TEAD1):c.525T>C (p.Phe175=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2011526	NM_021961.6(TEAD1):c.156A>T (p.Pro52=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1994117	NM_021961.6(TEAD1):c.483T>G (p.Ile161Met)	TEAD1 (I161M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1985846	NM_021961.6(TEAD1):c.496C>G (p.Pro166Ala)	TEAD1 (P166A)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1982359	NM_021961.6(TEAD1):c.1096A>G (p.Ile366Val)	TEAD1 (I366V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1978697	NM_021961.6(TEAD1):c.699+9G>T	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1978438	NM_021961.6(TEAD1):c.491G>T (p.Gly164Val)	TEAD1 (G164V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1978433	NM_021961.6(TEAD1):c.795A>G (p.Lys265=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1974876	NM_021961.6(TEAD1):c.1065C>T (p.Arg355=)	TEAD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1968228	NM_021961.6(TEAD1):c.887G>A (p.Cys296Tyr)	TEAD1 (C296Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1965626	NM_021961.6(TEAD1):c.686G>A (p.Arg229Gln)	TEAD1 (R229Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1957197	NM_021961.6(TEAD1):c.268-14C>T	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1956974	NM_021961.6(TEAD1):c.1167+19T>C	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1952427	NM_021961.6(TEAD1):c.465+17G>T	TEAD1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1945041	NM_021961.6(TEAD1):c.575G>T (p.Gly192Val)	TEAD1 (G192V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1943165	NM_021961.6(TEAD1):c.937G>A (p.Glu313Lys)	TEAD1 (E313K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

<< First< Prev

Page of 3