"Ambry Genetics"[submitter] AND "IFIT1"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3108170	NM_001548.5(IFIT1):c.7A>C (p.Thr3Pro)	IFIT1 (T3P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598362	NM_001548.5(IFIT1):c.17A>T (p.Asp6Val)	IFIT1 (D6V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108164	NM_001548.5(IFIT1):c.31A>G (p.Lys11Glu)	IFIT1 (K11E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588686	NM_001548.5(IFIT1):c.43G>C (p.Glu15Gln)	IFIT1 (E15Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493084	NM_001548.5(IFIT1):c.149A>G (p.Tyr50Cys)	IFIT1 (Y19C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524766	NM_001548.5(IFIT1):c.163C>T (p.His55Tyr)	IFIT1 (H55Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219951	NM_001548.5(IFIT1):c.290C>T (p.Thr97Ile)	IFIT1 (T97I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358367	NM_001548.5(IFIT1):c.341C>T (p.Ala114Val)	IFIT1 (A83V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398422	NM_001548.5(IFIT1):c.365A>G (p.Glu122Gly)	IFIT1 (E122G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239049	NM_001548.5(IFIT1):c.398G>A (p.Arg133His)	IFIT1 (R133H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519356	NM_001548.5(IFIT1):c.427T>C (p.Cys143Arg)	IFIT1 (C112R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108165	NM_001548.5(IFIT1):c.476G>A (p.Arg159Gln)	IFIT1 (R128Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285318	NM_001548.5(IFIT1):c.508G>A (p.Val170Met)	IFIT1 (V139M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516949	NM_001548.5(IFIT1):c.545C>T (p.Ala182Val)	IFIT1 (A151V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108166	NM_001548.5(IFIT1):c.613C>T (p.Pro205Ser)	IFIT1 (P174S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108167	NM_001548.5(IFIT1):c.665T>G (p.Leu222Arg)	IFIT1 (L191R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461836	NM_001548.5(IFIT1):c.730C>G (p.Leu244Val)	IFIT1 (L213V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108168	NM_001548.5(IFIT1):c.748C>G (p.Gln250Glu)	IFIT1 (Q219E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108169	NM_001548.5(IFIT1):c.770C>T (p.Ala257Val)	IFIT1 (A226V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204072	NM_001548.5(IFIT1):c.779T>A (p.Phe260Tyr)	IFIT1 (F229Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566210	NM_001548.5(IFIT1):c.785G>A (p.Arg262Gln)	IFIT1 (R262Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239766	NM_001548.5(IFIT1):c.808G>A (p.Ala270Thr)	IFIT1 (A270T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325739	NM_001548.5(IFIT1):c.832T>G (p.Leu278Val)	IFIT1 (L247V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210118	NM_001548.5(IFIT1):c.933A>T (p.Arg311Ser)	IFIT1 (R280S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108160	NM_001548.5(IFIT1):c.1039G>A (p.Ala347Thr)	IFIT1 (A316T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108161	NM_001548.5(IFIT1):c.1042A>G (p.Arg348Gly)	IFIT1 (R317G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108162	NM_001548.5(IFIT1):c.1049A>G (p.Tyr350Cys)	IFIT1 (Y350C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285319	NM_001548.5(IFIT1):c.1167A>C (p.Glu389Asp)	IFIT1 (E358D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108163	NM_001548.5(IFIT1):c.1181C>A (p.Ser394Tyr)	IFIT1 (S394Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 29