Related gene-specific medical variations for Gene (Select 3178) - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3361897	NM_031157.4(HNRNPA1):c.145C>A (p.Pro49Thr)	HNRNPA1 (P49T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3256957	NM_031157.4(HNRNPA1):c.16-4C>G	HNRNPA1, LOC117038776	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3058851	NM_031157.4(HNRNPA1):c.213T>C (p.Ala71=)	HNRNPA1, LOC117038776	Single nucleotide variant (synonymous variant +1 more)	HNRNPA1-related disorder	GLikely benign
Select item 3048056	NM_031157.4(HNRNPA1):c.279+9G>A	HNRNPA1, LOC117038776	Single nucleotide variant (intron variant)	HNRNPA1-related disorder	GLikely benign
Select item 3043203	NM_031157.4(HNRNPA1):c.279+10T>G	HNRNPA1, LOC117038776	Single nucleotide variant (intron variant)	HNRNPA1-related disorder	GLikely benign
Select item 2689217	NM_031157.4(HNRNPA1):c.914A>G (p.Asn305Ser)	HNRNPA1 (N253S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2683801	NM_031157.4(HNRNPA1):c.1113_*2delinsTAA (p.Arg371_Ter373delinsSerXaa)	HNRNPA1	Indel (stop lost +1 more)	Distal myopathy	GLikely pathogenic
Select item 2683203	NM_031157.4(HNRNPA1):c.11C>T (p.Ser4Leu)	HNRNPA1, LOC117038776 (S4L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432504	NM_031157.4(HNRNPA1):c.703G>A (p.Gly235Ser)	HNRNPA1 (G235S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432502	NM_031157.4(HNRNPA1):c.959A>T (p.Asn320Ile)	HNRNPA1 (N268I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432501	NM_031157.4(HNRNPA1):c.809G>T (p.Gly270Val)	HNRNPA1 (G270V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432500	NM_031157.4(HNRNPA1):c.648C>G (p.Phe216Leu)	HNRNPA1 (F216L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432499	NM_031157.4(HNRNPA1):c.1066G>A (p.Gly356Ser)	HNRNPA1 (G304S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432498	NM_031157.4(HNRNPA1):c.127dup (p.Cys43fs)	HNRNPA1, LOC117038776 (C43fs)	Duplication (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2432497	NM_031157.4(HNRNPA1):c.889G>A (p.Gly297Ser)	HNRNPA1 (G297S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432496	NM_031157.4(HNRNPA1):c.1027G>A (p.Gly343Ser)	HNRNPA1 (G291S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432495	NM_031157.4(HNRNPA1):c.959A>G (p.Asn320Ser)	HNRNPA1 (N268S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432494	NM_031157.4(HNRNPA1):c.873C>G (p.Asn291Lys)	HNRNPA1 (N291K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2432493	NM_031157.4(HNRNPA1):c.874_877dup (p.Gly293fs)	HNRNPA1 (G293fs)	Duplication (frameshift variant +1 more)	not provided	GUncertain significance
Select item 1333611	NM_031157.4(HNRNPA1):c.240_243del (p.Asp80fs)	HNRNPA1, LOC117038776 (D80fs)	Microsatellite (frameshift variant +1 more)	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3	GUncertain significance
Select item 1281374	NM_031157.4(HNRNPA1):c.16-57G>A	HNRNPA1, LOC117038776	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 797107	NM_031157.4(HNRNPA1):c.90G>A (p.Leu30=)	HNRNPA1, LOC117038776	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 789414	NM_031157.4(HNRNPA1):c.24A>G (p.Lys8=)	HNRNPA1, LOC117038776	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 705385	NM_031157.4(HNRNPA1):c.15+7T>C	HNRNPA1, LOC117038776	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 261941	NM_031157.4(HNRNPA1):c.133-17A>G	HNRNPA1, LOC117038776	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 135615	NM_031157.4(HNRNPA1):c.1114T>C (p.Phe372Leu)	HNRNPA1 (F372L +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely benign
Select item 135614	NM_031157.4(HNRNPA1):c.1111A>G (p.Arg371Gly)	HNRNPA1 (R371G +1 more)	Single nucleotide variant (missense variant +1 more)	Relapsing remitting multiple sclerosis	GLikely benign
Select item 135613	NM_031157.4(HNRNPA1):c.1106G>A (p.Gly369Asp)	HNRNPA1 (G369D +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely benign
Select item 135612	NM_031157.4(HNRNPA1):c.1097A>G (p.Tyr366Cys)	HNRNPA1 (Y366C +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely benign
Select item 135611	NM_031157.4(HNRNPA1):c.1096T>C (p.Tyr366His)	HNRNPA1 (Y366H +1 more)	Single nucleotide variant (missense variant +1 more)	Relapsing remitting multiple sclerosis	GLikely benign
Select item 135610	NM_031157.4(HNRNPA1):c.1093A>G (p.Ser365Gly)	HNRNPA1 (S365G +1 more)	Single nucleotide variant (missense variant +1 more)	Relapsing remitting multiple sclerosis	GLikely benign
Select item 135609	NM_031157.4(HNRNPA1):c.1078T>G (p.Ser360Ala)	HNRNPA1 (S360A +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely benign
Select item 135608	NM_031157.4(HNRNPA1):c.1058A>G (p.Asn353Ser)	HNRNPA1 (N353S +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135607	NM_031157.4(HNRNPA1):c.1057A>G (p.Asn353Asp)	HNRNPA1 (N353D +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135606	NM_031157.4(HNRNPA1):c.1054C>T (p.Arg352Ter)	HNRNPA1 (R352* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 135605	NM_031157.4(HNRNPA1):c.1052C>T (p.Pro351Leu)	HNRNPA1 (P351L +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135604	NM_031157.4(HNRNPA1):c.1042T>C (p.Phe348Leu)	HNRNPA1 (F348L +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135603	NM_031157.4(HNRNPA1):c.1040A>G (p.Tyr347Cys)	HNRNPA1 (Y347C +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135602	NM_031157.4(HNRNPA1):c.1009A>G (p.Ser337Gly)	HNRNPA1 (S337G +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135601	NM_031157.4(HNRNPA1):c.1006A>G (p.Arg336Gly)	HNRNPA1 (R336G +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135600	NM_031157.4(HNRNPA1):c.997T>C (p.Phe333Leu)	HNRNPA1 (F333L +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GPathogenic
Select item 135599	NM_031157.4(HNRNPA1):c.995A>G (p.Asn332Ser)	HNRNPA1 (N332S +1 more)	Single nucleotide variant (missense variant +1 more)	Relapsing remitting multiple sclerosis	GLikely pathogenic
Select item 135598	NM_031157.4(HNRNPA1):c.987G>T (p.Lys329Asn)	HNRNPA1 (K329N +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135597	NM_031157.4(HNRNPA1):c.982A>C (p.Met328Leu)	HNRNPA1 (M328L +1 more)	Single nucleotide variant (missense variant +1 more)	Relapsing remitting multiple sclerosis	GLikely pathogenic
Select item 135596	NM_031157.4(HNRNPA1):c.979C>T (p.Pro327Ser)	HNRNPA1 (P327S +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135595	NM_031157.4(HNRNPA1):c.973T>G (p.Phe325Val)	HNRNPA1 (F325V +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GPathogenic
Select item 135594	NM_031157.4(HNRNPA1):c.973T>C (p.Phe325Leu)	HNRNPA1 (F325L +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GPathogenic
Select item 135593	NM_031157.4(HNRNPA1):c.949A>G (p.Asn317Asp)	HNRNPA1 (N317D +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135592	NM_031157.4(HNRNPA1):c.943T>C (p.Phe315Leu)	HNRNPA1 (F315L +1 more)	Single nucleotide variant (missense variant +1 more)	Chronic progressive multiple sclerosis	GLikely pathogenic
Select item 135591	NM_031157.4(HNRNPA1):c.931A>G (p.Ser311Gly)	HNRNPA1 (S311G +1 more)	Single nucleotide variant (missense variant +1 more)	Relapsing remitting multiple sclerosis	GUncertain significance
Select item 135590	NM_031157.4(HNRNPA1):c.911G>A (p.Ser304Asn)	HNRNPA1 (S304N +1 more)	Single nucleotide variant (missense variant +1 more)	Relapsing remitting multiple sclerosis	GUncertain significance

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Links from Gene

Items: 51