"Ambry Genetics"[submitter] AND "LY9"[gene] - ClinVar

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Items: 48

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2318119	NM_002348.4(LY9):c.98A>C (p.Gln33Pro)	LY9 (Q33P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121637	NM_002348.4(LY9):c.114C>G (p.Phe38Leu)	LY9 (F38L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253232	NM_002348.4(LY9):c.151G>A (p.Ala51Thr)	LY9 (A51T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208499	NM_002348.4(LY9):c.173T>C (p.Ile58Thr)	LY9 (I58T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269970	NM_002348.4(LY9):c.218C>T (p.Thr73Ile)	LY9 (T73I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244291	NM_002348.4(LY9):c.269C>T (p.Ala90Val)	LY9 (A90V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121642	NM_002348.4(LY9):c.271C>T (p.Arg91Cys)	LY9 (R91C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121643	NM_002348.4(LY9):c.282A>C (p.Glu94Asp)	LY9 (E94D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121644	NM_002348.4(LY9):c.290C>A (p.Thr97Asn)	LY9 (T97N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388073	NM_002348.4(LY9):c.350G>A (p.Cys117Tyr)	LY9 (C117Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456536	NM_002348.4(LY9):c.464A>G (p.Gln155Arg)	LY9 (Q155R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278672	NM_002348.4(LY9):c.531G>A (p.Met177Ile)	LY9 (M177I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614428	NM_002348.4(LY9):c.535T>G (p.Ser179Ala)	LY9 (S179A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511878	NM_002348.4(LY9):c.544G>A (p.Gly182Arg)	LY9 (G182R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400335	NM_002348.4(LY9):c.557G>C (p.Ser186Thr)	LY9 (S186T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292363	NM_002348.4(LY9):c.632G>A (p.Arg211Gln)	LY9 (R211Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292361	NM_002348.4(LY9):c.682G>A (p.Val228Ile)	LY9 (V228I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595297	NM_002348.4(LY9):c.707T>C (p.Val236Ala)	LY9 (V236A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276608	NM_002348.4(LY9):c.772G>T (p.Val258Leu)	LY9 (V258L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390259	NM_002348.4(LY9):c.824G>A (p.Arg275Gln)	LY9 (R275Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2374624	NM_002348.4(LY9):c.841G>A (p.Val281Ile)	LY9 (V281I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121645	NM_002348.4(LY9):c.877A>G (p.Arg293Gly)	LY9 (R293G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589870	NM_002348.4(LY9):c.919G>C (p.Asp307His)	LY9 (D307H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374646	NM_002348.4(LY9):c.1097C>T (p.Thr366Met)	LY9 (T366M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551532	NM_002348.4(LY9):c.1103G>T (p.Ser368Ile)	LY9 (S368I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2569527	NM_002348.4(LY9):c.1105C>T (p.Leu369Phe)	LY9 (L369F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529146	NM_002348.4(LY9):c.1121A>T (p.Asp374Val)	LY9 (D374V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121638	NM_002348.4(LY9):c.1162G>A (p.Gly388Arg)	LY9 (G388R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519429	NM_002348.4(LY9):c.1169A>T (p.Asn390Ile)	LY9 (N390I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611028	NM_002348.4(LY9):c.1227A>C (p.Glu409Asp)	LY9 (E409D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304551	NM_002348.4(LY9):c.1310C>G (p.Ser437Cys)	LY9 (S437C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617691	NM_002348.4(LY9):c.1321C>A (p.Leu441Ile)	LY9 (L441I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121639	NM_002348.4(LY9):c.1403T>C (p.Val468Ala)	LY9 (V378A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324156	NM_002348.4(LY9):c.1462T>C (p.Cys488Arg)	LY9 (C398R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227351	NM_002348.4(LY9):c.1487C>T (p.Ala496Val)	LY9 (A496V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252262	NM_002348.4(LY9):c.1561C>A (p.Pro521Thr)	LY9 (P431T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290822	NM_002348.4(LY9):c.1571C>T (p.Pro524Leu)	LY9 (P524L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292360	NM_002348.4(LY9):c.1577G>C (p.Arg526Thr)	LY9 (R512T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292366	NM_002348.4(LY9):c.1591C>A (p.Pro531Thr)	LY9 (P441T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589673	NM_002348.4(LY9):c.1670G>A (p.Ser557Asn)	LY9 (S543N +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2591146	NM_002348.4(LY9):c.1689T>A (p.Phe563Leu)	LY9 (F473L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121640	NM_002348.4(LY9):c.1712C>G (p.Ala571Gly)	LY9 (A481G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266691	NM_002348.4(LY9):c.1714G>A (p.Gly572Arg)	LY9 (G482R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292362	NM_002348.4(LY9):c.1721A>G (p.Asp574Gly)	LY9 (D560G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292365	NM_002348.4(LY9):c.1789G>T (p.Val597Phe)	LY9 (V597F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262479	NM_002348.4(LY9):c.1805T>C (p.Met602Thr)	LY9 (M588T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250619	NM_002348.4(LY9):c.1860G>C (p.Glu620Asp)	LY9 (E530D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121641	NM_002348.4(LY9):c.1915C>G (p.Gln639Glu)	LY9 (Q625E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 48