ClinVar for Gene (Select 6775) - ClinVar - NCBI

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

Links from Gene

Items: 1 to 100 of 402

<< First< Prev

Page of 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3350703	NM_003151.4(STAT4):c.1516G>A (p.Val506Ile)	STAT4 (V506I)	Single nucleotide variant (missense variant)	STAT4-related disorder	GUncertain significance
Select item 3323184	NM_003151.4(STAT4):c.305C>G (p.Ala102Gly)	STAT4 (A102G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3239489	NM_003151.4(STAT4):c.1641A>G (p.Ser547=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3171118	NM_003151.4(STAT4):c.662A>G (p.His221Arg)	STAT4 (H221R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171117	NM_003151.4(STAT4):c.590C>A (p.Thr197Lys)	STAT4 (T197K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171116	NM_003151.4(STAT4):c.436A>C (p.Lys146Gln)	STAT4 (K146Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171115	NM_003151.4(STAT4):c.1873G>A (p.Val625Ile)	STAT4 (V625I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060199	NM_003151.4(STAT4):c.129-3dup	STAT4	Duplication (intron variant)	STAT4-related disorder	GBenign
Select item 3023241	NM_003151.4(STAT4):c.477A>G (p.Gln159=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3022851	NM_003151.4(STAT4):c.183A>G (p.Leu61=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3018599	NM_003151.4(STAT4):c.2014G>A (p.Gly672Ser)	STAT4 (G672S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3010310	NM_003151.4(STAT4):c.942-1G>C	STAT4	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 3008667	NM_003151.4(STAT4):c.1570+1G>A	STAT4	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 3007384	NM_003151.4(STAT4):c.274-14G>T	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006008	NM_003151.4(STAT4):c.1452T>C (p.Asn484=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004553	NM_003151.4(STAT4):c.1852+9T>G	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004501	NM_003151.4(STAT4):c.1413C>T (p.Asn471=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 3002446	NM_003151.4(STAT4):c.1620+20C>A	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3001422	NM_003151.4(STAT4):c.346T>C (p.Leu116=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2996758	NM_003151.4(STAT4):c.1411A>C (p.Asn471His)	STAT4 (N471H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2995883	NM_003151.4(STAT4):c.2112-16T>G	STAT4, STAT4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2994626	NM_003151.4(STAT4):c.861A>G (p.Thr287=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2988312	NM_003151.4(STAT4):c.2044+18_2044+21del	STAT4	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2987715	NM_003151.4(STAT4):c.1512G>A (p.Ser504=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2982964	NM_003151.4(STAT4):c.1035-19dup	STAT4	Duplication (intron variant)	not provided	GBenign
Select item 2981550	NM_003151.4(STAT4):c.630+17A>C	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2981234	NM_003151.4(STAT4):c.1095-16C>A	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978311	NM_003151.4(STAT4):c.1853-5del	STAT4	Deletion (intron variant)	not provided	GBenign
Select item 2977997	NM_003151.4(STAT4):c.544+7T>G	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2976288	NM_003151.4(STAT4):c.1059A>C (p.Leu353=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2975189	NM_003151.4(STAT4):c.727C>A (p.Gln243Lys)	STAT4 (Q243K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2965000	NM_003151.4(STAT4):c.1937A>G (p.Lys646Arg)	STAT4 (K646R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2962777	NM_003151.4(STAT4):c.1259A>T (p.His420Leu)	STAT4 (H420L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2962303	NM_003151.4(STAT4):c.1570+18G>C	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960387	NM_003151.4(STAT4):c.527A>G (p.Lys176Arg)	STAT4 (K176R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2911762	NM_003151.4(STAT4):c.1927C>A (p.Arg643=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2905462	NM_003151.4(STAT4):c.2151T>G (p.Leu717=)	STAT4, STAT4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2896213	NM_003151.4(STAT4):c.763C>T (p.Leu255Phe)	STAT4 (L255F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2895266	NM_003151.4(STAT4):c.1483C>T (p.Leu495=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2895023	NM_003151.4(STAT4):c.1852+6T>C	STAT4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2893119	NM_003151.4(STAT4):c.1790T>C (p.Leu597Ser)	STAT4 (L597S)	Single nucleotide variant (missense variant)	Disabling pansclerotic morphea of childhood +1 more	GUncertain significance
Select item 2893077	NM_003151.4(STAT4):c.615C>T (p.Leu205=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2892929	NM_003151.4(STAT4):c.482C>T (p.Thr161Ile)	STAT4 (T161I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2885869	NM_003151.4(STAT4):c.469A>G (p.Thr157Ala)	STAT4 (T157A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2878961	NM_003151.4(STAT4):c.1043T>C (p.Ile348Thr)	STAT4 (I348T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2873335	NM_003151.4(STAT4):c.2112-17C>G	STAT4, STAT4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2867679	NM_003151.4(STAT4):c.319A>G (p.Asn107Asp)	STAT4 (N107D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2865983	NM_003151.4(STAT4):c.63C>A (p.Phe21Leu)	STAT4 (F21L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2862266	NM_003151.4(STAT4):c.1722C>G (p.Val574=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2849334	NM_003151.4(STAT4):c.129-14_129-13insG	STAT4	Insertion (intron variant)	not provided	GLikely benign
Select item 2848854	NM_003151.4(STAT4):c.367G>T (p.Val123Phe)	STAT4 (V123F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2845889	NM_003151.4(STAT4):c.630+7G>A	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2843001	NM_003151.4(STAT4):c.160A>G (p.Thr54Ala)	STAT4 (T54A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2836514	NM_003151.4(STAT4):c.1434+16A>G	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2831545	NM_003151.4(STAT4):c.1876G>C (p.Glu626Gln)	STAT4 (E626Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2831058	NM_003151.4(STAT4):c.2172G>T (p.Val724=)	STAT4, STAT4-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2830655	NM_003151.4(STAT4):c.1715+5G>A	STAT4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2827414	NM_003151.4(STAT4):c.1758_1759delinsTT (p.Leu586Phe)	STAT4 (L586F)	Indel (missense variant)	not provided	GUncertain significance
Select item 2820537	NM_003151.4(STAT4):c.1336-9C>A	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2817328	NM_003151.4(STAT4):c.1571-11T>C	STAT4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2814903	NM_003151.4(STAT4):c.924C>T (p.Ile308=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2814312	NM_003151.4(STAT4):c.1680A>G (p.Leu560=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2811383	NM_003151.4(STAT4):c.1045A>C (p.Lys349Gln)	STAT4 (K349Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2802978	NM_003151.4(STAT4):c.1930G>A (p.Asp644Asn)	STAT4 (D644N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2802766	NM_003151.4(STAT4):c.102G>A (p.Leu34=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2800995	NM_003151.4(STAT4):c.2207C>A (p.Thr736Lys)	STAT4, STAT4-AS1 (T736K)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2800634	NM_003151.4(STAT4):c.751C>T (p.Leu251Phe)	STAT4 (L251F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2796294	NM_003151.4(STAT4):c.630G>A (p.Lys210=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2787598	NM_003151.4(STAT4):c.1094+16del	STAT4	Deletion (intron variant)	not provided	GLikely benign
Select item 2783993	NM_003151.4(STAT4):c.1570+16_1570+19del	STAT4	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2783988	NM_003151.4(STAT4):c.1716-9T>C	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2782751	NM_003151.4(STAT4):c.631-15C>A	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2782650	NM_003151.4(STAT4):c.631-17G>T	STAT4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2782379	NM_003151.4(STAT4):c.942-6del	STAT4	Deletion (intron variant)	not provided	GLikely benign
Select item 2781730	NM_003151.4(STAT4):c.783-6C>T	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2779990	NM_003151.4(STAT4):c.942-11T>G	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2773021	NM_003151.4(STAT4):c.531A>C (p.Thr177=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2766455	NM_003151.4(STAT4):c.1886A>G (p.Asn629Ser)	STAT4 (N629S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2764884	NM_003151.4(STAT4):c.670G>T (p.Asp224Tyr)	STAT4 (D224Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2758256	NM_003151.4(STAT4):c.252A>G (p.Lys84=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2757256	NM_003151.4(STAT4):c.671A>C (p.Asp224Ala)	STAT4 (D224A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2755198	NM_003151.4(STAT4):c.240A>T (p.Ile80=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2750173	NM_003151.4(STAT4):c.1761A>G (p.Leu587=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2749548	NM_003151.4(STAT4):c.1621-19T>G	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2747227	NM_003151.4(STAT4):c.100T>C (p.Leu34=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2742725	NM_003151.4(STAT4):c.949G>A (p.Val317Met)	STAT4 (V317M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2730791	NM_003151.4(STAT4):c.2174A>G (p.Tyr725Cys)	STAT4, STAT4-AS1 (Y725C)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2726505	NM_003151.4(STAT4):c.291T>A (p.Asn97Lys)	STAT4 (N97K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2719850	NM_003151.4(STAT4):c.1113-15A>T	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2719846	NM_003151.4(STAT4):c.703C>T (p.Leu235=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2716800	NM_003151.4(STAT4):c.550A>G (p.Ser184Gly)	STAT4 (S184G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2715525	NM_003151.4(STAT4):c.14A>G (p.Asn5Ser)	STAT4 (N5S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2714066	NM_003151.4(STAT4):c.519C>T (p.Tyr173=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2704368	NM_003151.4(STAT4):c.1336-13C>T	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2702721	NM_003151.4(STAT4):c.435C>T (p.His145=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2697417	NM_003151.4(STAT4):c.1034+20A>T	STAT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2695509	NM_003151.4(STAT4):c.470C>G (p.Thr157Arg)	STAT4 (T157R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2694950	NM_003151.4(STAT4):c.930C>T (p.Asn310=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2693201	NM_003151.4(STAT4):c.1643_1651del (p.Phe548_Phe550del)	STAT4	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2692881	NM_003151.4(STAT4):c.1857A>G (p.Glu619=)	STAT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

<< First< Prev

Page of 5