"Invitae"[submitter] AND "IRF4"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2852933	NM_002460.4(IRF4):c.2T>G (p.Met1Arg)	IRF4 (M1R)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 1555544	NM_002460.4(IRF4):c.6C>T (p.Asn2=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2729493	NM_002460.4(IRF4):c.7C>T (p.Leu3=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2780101	NM_002460.4(IRF4):c.14G>A (p.Gly5Asp)	IRF4 (G5D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2968043	NM_002460.4(IRF4):c.16G>C (p.Gly6Arg)	IRF4 (G6R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1395491	NM_002460.4(IRF4):c.20G>A (p.Gly7Asp)	IRF4 (G7D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1414544	NM_002460.4(IRF4):c.23G>A (p.Arg8Gln)	IRF4 (R8Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1390195	NM_002460.4(IRF4):c.23G>T (p.Arg8Leu)	IRF4 (R8L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1634528	NM_002460.4(IRF4):c.27C>T (p.Gly9=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1351821	NM_002460.4(IRF4):c.36C>G (p.Phe12Leu)	IRF4 (F12L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2790560	NM_002460.4(IRF4):c.39C>T (p.Gly13=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2127608	NM_002460.4(IRF4):c.41T>C (p.Met14Thr)	IRF4 (M14T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2969143	NM_002460.4(IRF4):c.53G>A (p.Ser18Asn)	IRF4 (S18N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2896292	NM_002460.4(IRF4):c.53G>C (p.Ser18Thr)	IRF4 (S18T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1958125	NM_002460.4(IRF4):c.66G>A (p.Gly22=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1383762	NM_002460.4(IRF4):c.73C>G (p.Arg25Gly)	IRF4 (R25G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1484917	NM_002460.4(IRF4):c.75C>T (p.Arg25=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1461971	NM_002460.4(IRF4):c.86T>G (p.Ile29Ser)	IRF4 (I29S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1717885	NM_002460.4(IRF4):c.91C>G (p.Gln31Glu)	IRF4 (Q31E)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2177075	NM_002460.4(IRF4):c.112C>T (p.Pro38Ser)	IRF4 (P38S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1532310	NM_002460.4(IRF4):c.120G>A (p.Leu40=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2964784	NM_002460.4(IRF4):c.129G>A (p.Glu43=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2959792	NM_002460.4(IRF4):c.133G>C (p.Glu45Gln)	IRF4 (E45Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1954294	NM_002460.4(IRF4):c.133GAG[1] (p.Glu46del)	IRF4 (E46del)	Microsatellite (inframe_deletion +1 more)	not provided	GUncertain significance
Select item 1555026	NM_002460.4(IRF4):c.165G>A (p.Lys55=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1569627	NM_002460.4(IRF4):c.171G>T (p.Ala57=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1370374	NM_002460.4(IRF4):c.183C>G (p.Asp61Glu)	IRF4 (D61E)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2805618	NM_002460.4(IRF4):c.207G>A (p.Ala69=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1169632	NM_002460.4(IRF4):c.207G>C (p.Ala69=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1621912	NM_002460.4(IRF4):c.216+7G>A	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2855650	NM_002460.4(IRF4):c.216+9C>T	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959695	NM_002460.4(IRF4):c.216+20G>T	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3023979	NM_002460.4(IRF4):c.217-20T>G	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1583999	NM_002460.4(IRF4):c.217-19C>T	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881558	NM_002460.4(IRF4):c.219T>G (p.Ala73=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1406322	NM_002460.4(IRF4):c.234A>G (p.Lys78=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2863460	NM_002460.4(IRF4):c.244C>T (p.Arg82Ter)	IRF4 (R82*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 1919325	NM_002460.4(IRF4):c.262C>G (p.Pro88Ala)	IRF4 (P88A)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1116007	NM_002460.4(IRF4):c.263C>A (p.Pro88Gln)	IRF4 (P88Q)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1657878	NM_002460.4(IRF4):c.264G>A (p.Pro88=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1639618	NM_002460.4(IRF4):c.276C>G (p.Thr92=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2987365	NM_002460.4(IRF4):c.284C>G (p.Thr95Arg)	IRF4 (T95R)	Single nucleotide variant (missense variant +1 more)	not provided	GPathogenic
Select item 2106324	NM_002460.4(IRF4):c.284C>T (p.Thr95Met)	IRF4 (T95M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1642510	NM_002460.4(IRF4):c.285G>A (p.Thr95=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2047929	NM_002460.4(IRF4):c.287G>C (p.Arg96Pro)	IRF4 (R96P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1557594	NM_002460.4(IRF4):c.294G>T (p.Arg98=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2811971	NM_002460.4(IRF4):c.297C>G (p.Cys99Trp)	IRF4 (C99W)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1604014	NM_002460.4(IRF4):c.297C>T (p.Cys99=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2129846	NM_002460.4(IRF4):c.309G>T (p.Lys103Asn)	IRF4 (K103N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2889516	NM_002460.4(IRF4):c.328C>A (p.Leu110Met)	IRF4 (L110M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2013810	NM_002460.4(IRF4):c.337C>T (p.Arg113Trp)	IRF4 (R113W)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1359527	NM_002460.4(IRF4):c.338G>A (p.Arg113Gln)	IRF4 (R113Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1579377	NM_002460.4(IRF4):c.354C>T (p.Ile118=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3007872	NM_002460.4(IRF4):c.363G>A (p.Pro121=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2815301	NM_002460.4(IRF4):c.365A>G (p.Tyr122Cys)	IRF4 (Y122C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2858938	NM_002460.4(IRF4):c.373T>C (p.Tyr125His)	IRF4 (Y125H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1478272	NM_002460.4(IRF4):c.377G>A (p.Arg126Lys)	IRF4 (R126K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2861379	NM_002460.4(IRF4):c.378G>T (p.Arg126Ser)	IRF4 (R126S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2815154	NM_002460.4(IRF4):c.403G>A (p.Gly135Arg)	IRF4 (G135R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2975166	NM_002460.4(IRF4):c.403+2T>C	IRF4	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 2777972	NM_002460.4(IRF4):c.403+4G>C	IRF4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1536168	NM_002460.4(IRF4):c.403+9T>G	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1553625	NM_002460.4(IRF4):c.403+13C>T	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2853821	NM_002460.4(IRF4):c.403+18T>C	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1927787	NM_002460.4(IRF4):c.404-13C>T	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2872221	NM_002460.4(IRF4):c.404-9A>T	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1497416	NM_002460.4(IRF4):c.407C>T (p.Ala136Val)	IRF4 (A136V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1637555	NM_002460.4(IRF4):c.420C>G (p.Thr140=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1039904	NM_002460.4(IRF4):c.421C>G (p.Leu141Val)	IRF4 (L141V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2135911	NM_002460.4(IRF4):c.432G>T (p.Pro144=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1528733	NM_002460.4(IRF4):c.432G>A (p.Pro144=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2083932	NM_002460.4(IRF4):c.438G>A (p.Met146Ile)	IRF4 (M146I)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 792028	NM_002460.4(IRF4):c.446G>A (p.Ser149Asn)	IRF4 (S149N)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1616018	NM_002460.4(IRF4):c.447C>T (p.Ser149=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1515825	NM_002460.4(IRF4):c.448C>T (p.His150Tyr)	IRF4 (H150Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2089318	NM_002460.4(IRF4):c.459C>G (p.Thr153=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2786884	NM_002460.4(IRF4):c.467C>T (p.Thr156Met)	IRF4 (T156M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2752910	NM_002460.4(IRF4):c.468G>A (p.Thr156=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1560653	NM_002460.4(IRF4):c.468G>T (p.Thr156=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2709414	NM_002460.4(IRF4):c.469C>T (p.Pro157Ser)	IRF4 (P157S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1564323	NM_002460.4(IRF4):c.480G>A (p.Ser160=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2088295	NM_002460.4(IRF4):c.483C>G (p.Leu161=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2805058	NM_002460.4(IRF4):c.492+11G>A	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1166330	NM_002460.4(IRF4):c.493-7C>T	IRF4	Single nucleotide variant (intron variant)	IRF4-related condition +1 more	GBenign/Likely benign
Select item 2743758	NM_002460.4(IRF4):c.493-5T>G	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1930920	NM_002460.4(IRF4):c.493-4T>G	IRF4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1500131	NM_002460.4(IRF4):c.493-3T>C	IRF4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2193290	NM_002460.4(IRF4):c.500A>G (p.His167Arg)	IRF4 (H167R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2859258	NM_002460.4(IRF4):c.501C>G (p.His167Gln)	IRF4 (H166Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1660793	NM_002460.4(IRF4):c.507C>T (p.Tyr169=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1346527	NM_002460.4(IRF4):c.512T>C (p.Met171Thr)	IRF4 (M171T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3006621	NM_002460.4(IRF4):c.517C>A (p.Pro173Thr)	IRF4 (P172T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1158809	NM_002460.4(IRF4):c.522C>T (p.Leu174=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2050852	NM_002460.4(IRF4):c.523G>T (p.Asp175Tyr)	IRF4 (D175Y +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2877004	NM_002460.4(IRF4):c.527G>A (p.Arg176Gln)	IRF4 (R176Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1409983	NM_002460.4(IRF4):c.541T>C (p.Tyr181His)	IRF4 (Y180H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2869543	NM_002460.4(IRF4):c.542A>G (p.Tyr181Cys)	IRF4 (Y181C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1909524	NM_002460.4(IRF4):c.543C>T (p.Tyr181=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1467405	NM_002460.4(IRF4):c.548C>T (p.Pro183Leu)	IRF4 (P182L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1666714	NM_002460.4(IRF4):c.549G>A (p.Pro183=)	IRF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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