Related gene-specific medical variations for Gene (Select 51266) - ClinVar

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Links from Gene

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3267680	NM_016509.4(CLEC1B):c.184C>G (p.Leu62Val)	CLEC12A, CLEC1B (L29V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267679	NM_016509.4(CLEC1B):c.91C>T (p.Arg31Cys)	CLEC12A, CLEC1B (R31C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3267678	NM_016509.4(CLEC1B):c.250G>C (p.Val84Leu)	CLEC12A, CLEC1B (V51L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3145649	NM_016509.4(CLEC1B):c.77C>T (p.Ser26Phe)	CLEC12A, CLEC1B (S26F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145648	NM_016509.4(CLEC1B):c.566G>C (p.Gly189Ala)	CLEC12A, CLEC1B (G189A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145647	NM_016509.4(CLEC1B):c.379A>G (p.Lys127Glu)	CLEC12A, CLEC1B (K127E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145646	NM_016509.4(CLEC1B):c.353G>C (p.Arg118Thr)	CLEC12A, CLEC1B (R118T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145645	NM_016509.4(CLEC1B):c.341A>T (p.Tyr114Phe)	CLEC12A, CLEC1B (Y114F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145644	NM_016509.4(CLEC1B):c.320G>A (p.Arg107Lys)	CLEC12A, CLEC1B (R107K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145643	NM_016509.4(CLEC1B):c.236G>T (p.Arg79Leu)	CLEC12A, CLEC1B (R46L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145642	NM_016509.4(CLEC1B):c.228A>T (p.Leu76Phe)	CLEC12A, CLEC1B (L43F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145641	NM_016509.4(CLEC1B):c.223C>G (p.Gln75Glu)	CLEC12A, CLEC1B (Q42E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145640	NM_016509.4(CLEC1B):c.208A>G (p.Thr70Ala)	CLEC12A, CLEC1B (T70A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145639	NM_016509.4(CLEC1B):c.194A>G (p.Glu65Gly)	CLEC12A, CLEC1B (E32G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145637	NM_016509.4(CLEC1B):c.128G>T (p.Gly43Val)	CLEC12A, CLEC1B (G43V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145636	NM_016509.4(CLEC1B):c.100G>C (p.Ala34Pro)	CLEC12A, CLEC1B (A34P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599083	NM_016509.4(CLEC1B):c.286G>T (p.Gly96Cys)	CLEC12A, CLEC1B (G63C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555809	NM_016509.4(CLEC1B):c.100G>T (p.Ala34Ser)	CLEC12A, CLEC1B (A34S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495040	NM_016509.4(CLEC1B):c.205C>G (p.Arg69Gly)	CLEC12A, CLEC1B (R36G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488832	NM_016509.4(CLEC1B):c.575A>T (p.Asn192Ile)	CLEC12A, CLEC1B (N159I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406783	NM_016509.4(CLEC1B):c.665T>A (p.Met222Lys)	CLEC12A, CLEC1B (M222K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366472	NM_016509.4(CLEC1B):c.136G>T (p.Val46Phe)	CLEC12A, CLEC1B (V46F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352509	NM_016509.4(CLEC1B):c.236G>A (p.Arg79His)	CLEC12A, CLEC1B (R79H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318094	NM_016509.4(CLEC1B):c.181T>C (p.Tyr61His)	CLEC12A, CLEC1B (Y61H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301786	NM_016509.4(CLEC1B):c.187C>A (p.Gln63Lys)	CLEC12A, CLEC1B (Q63K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294999	NM_016509.4(CLEC1B):c.241T>A (p.Cys81Ser)	CLEC12A, CLEC1B (C48S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286219	NM_016509.4(CLEC1B):c.359A>G (p.Asn120Ser)	CLEC12A, CLEC1B (N87S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235779	NM_016509.4(CLEC1B):c.509G>C (p.Trp170Ser)	CLEC12A, CLEC1B (W137S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229921	NM_016509.4(CLEC1B):c.402T>G (p.Asn134Lys)	CLEC12A, CLEC1B (N101K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 29