C0393665[trait identifier] AND "Demyelinating Disease Laboratories, VA - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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