LY6E[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2608347	NM_002346.3(LY6E):c.59C>T (p.Ser20Leu)	LY6E (S20L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363497	NM_002346.3(LY6E):c.145G>A (p.Val49Met)	LY6E (V49M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121612	NM_002346.3(LY6E):c.241G>A (p.Val81Ile)	LY6E (V81I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2378393	NM_002346.3(LY6E):c.262A>T (p.Met88Leu)	LY6E (M88L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535556	NM_002346.3(LY6E):c.272G>C (p.Ser91Thr)	LY6E (S91T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782281	NM_002346.3(LY6E):c.306G>A (p.Ala102=)	LY6E	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 711022	NM_002346.3(LY6E):c.310G>A (p.Asp104Asn)	LY6E (D104N)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2527177	NM_002346.3(LY6E):c.312T>G (p.Asp104Glu)	LY6E (D104E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 788736	NM_002346.3(LY6E):c.315C>T (p.Gly105=)	LY6E	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2264557	NM_002346.3(LY6E):c.322C>T (p.Arg108Trp)	LY6E (R108W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527178	NM_002346.3(LY6E):c.325G>C (p.Ala109Pro)	LY6E (A109P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782282	NM_002346.3(LY6E):c.331G>A (p.Val111Ile)	LY6E (V111I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2336211	NM_002346.3(LY6E):c.371C>T (p.Pro124Leu)	LY6E (P124L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance