Related gene-specific medical variations for Gene (Select 110599563) - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3121625	NM_001003693.3(LY6G6F):c.809C>T (p.Ser270Leu)	LY6G6F, LY6G6F-LY6G6D (S270L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121624	NM_001003693.3(LY6G6F):c.787G>T (p.Gly263Trp)	LY6G6F, LY6G6F-LY6G6D (G263W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121623	NM_001003693.3(LY6G6F):c.709C>G (p.Leu237Val)	LY6G6F, LY6G6F-LY6G6D (L237V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121622	NM_001003693.3(LY6G6F):c.118A>G (p.Thr40Ala)	LY6G6F, LY6G6F-LY6G6D (T40A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121621	NM_021246.4(LY6G6D):c.397G>A (p.Gly133Arg)	LY6G6D, LY6G6F-LY6G6D (G133R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121620	NM_021246.4(LY6G6D):c.376C>A (p.Leu126Ile)	LY6G6D, LY6G6F-LY6G6D (L126I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599021	NM_001003693.3(LY6G6F):c.416C>A (p.Ser139Tyr)	LY6G6F, LY6G6F-LY6G6D (S139Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590333	NM_001003693.3(LY6G6F):c.133G>A (p.Glu45Lys)	LY6G6F, LY6G6F-LY6G6D (E45K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537380	NM_021246.4(LY6G6D):c.133G>A (p.Gly45Ser)	LY6G6D, LY6G6F-LY6G6D (G294S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521361	NM_001003693.3(LY6G6F):c.848A>G (p.Asn283Ser)	LY6G6F, LY6G6F-LY6G6D (N283S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517061	NM_001003693.3(LY6G6F):c.275G>C (p.Trp92Ser)	LY6G6F, LY6G6F-LY6G6D (W92S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514913	NM_001003693.3(LY6G6F):c.398C>T (p.Ala133Val)	LY6G6F, LY6G6F-LY6G6D (A133V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481654	NM_001003693.3(LY6G6F):c.226A>C (p.Lys76Gln)	LY6G6F, LY6G6F-LY6G6D (K76Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473304	NM_001003693.3(LY6G6F):c.313T>G (p.Trp105Gly)	LY6G6F, LY6G6F-LY6G6D (W105G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455889	NM_001003693.3(LY6G6F):c.497T>G (p.Val166Gly)	LY6G6F, LY6G6F-LY6G6D (V166G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454318	NM_021246.4(LY6G6D):c.74A>G (p.Tyr25Cys)	LY6G6D, LY6G6F-LY6G6D (Y25C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355064	NM_021246.4(LY6G6D):c.115G>A (p.Val39Met)	LY6G6D, LY6G6F-LY6G6D (V39M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343241	NM_001003693.3(LY6G6F):c.862C>T (p.Arg288Cys)	LY6G6F, LY6G6F-LY6G6D (R288C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272256	NM_001003693.3(LY6G6F):c.112C>T (p.Pro38Ser)	LY6G6F, LY6G6F-LY6G6D (P38S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262214	NM_001003693.3(LY6G6F):c.505C>T (p.Arg169Cys)	LY6G6F, LY6G6F-LY6G6D (R169C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255214	NM_001003693.3(LY6G6F):c.515C>T (p.Ser172Phe)	LY6G6F, LY6G6F-LY6G6D (S172F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249926	NM_021246.4(LY6G6D):c.137G>A (p.Arg46Lys)	LY6G6D, LY6G6F-LY6G6D (R295K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2228855	NM_001003693.3(LY6G6F):c.850A>T (p.Ile284Phe)	LY6G6F, LY6G6F-LY6G6D (I284F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222241	NM_021246.4(LY6G6D):c.217G>A (p.Ala73Thr)	LY6G6D, LY6G6F-LY6G6D (A73T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780983	NM_001003693.3(LY6G6F):c.101C>A (p.Pro34Gln)	LY6G6F, LY6G6F-LY6G6D (P34Q)	Single nucleotide variant (missense variant)	not provided	GBenign

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Items: 25