"Ambry Genetics"[submitter] AND "LY75"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2622879	NM_002349.4(LY75):c.5142G>C (p.Glu1714Asp)	LY75, LY75-CD302 (E1714D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121632	NM_002349.4(LY75):c.5120C>T (p.Ala1707Val)	LY75-CD302, LY75 (A1707V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595160	NM_001198759.1(LY75-CD302):c.2869C>T (p.Pro957Ser)	LY75, LY75-CD302 (P957S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518485	NM_002349.4(LY75):c.1735C>T (p.Arg579Trp)	LY75, LY75-CD302 (R579W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292356	NM_001198759.1(LY75-CD302):c.619G>A (p.Gly207Ser)	LY75, LY75-CD302 (G207S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121631	NM_002349.4(LY75):c.325A>C (p.Lys109Gln)	LY75, LY75-CD302 (K109Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455568	NM_002349.4(LY75):c.314T>C (p.Met105Thr)	LY75, LY75-CD302 (M105T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541012	NM_001198759.1(LY75-CD302):c.275T>G (p.Val92Gly)	LY75, LY75-CD302 (V92G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524433	NM_001198759.1(LY75-CD302):c.6G>C (p.Arg2Ser)	LY75, LY75-CD302 (R2S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance