"Ambry Genetics"[submitter] AND "LOC126863018"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2333905	NM_018677.4(ACSS2):c.1222A>G (p.Thr408Ala)	ACSS2, LOC126863018 (T421A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140933	NM_018677.4(ACSS2):c.1241G>A (p.Arg414His)	ACSS2, LOC126863018 (R414H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610372	NM_018677.4(ACSS2):c.1262A>T (p.Asp421Val)	ACSS2, LOC126863018 (D326V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316179	NM_018677.4(ACSS2):c.1286G>A (p.Arg429Gln)	ACSS2, LOC126863018 (R429Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140948	NM_018677.4(ACSS2):c.1366G>T (p.Ala456Ser)	ACSS2, LOC126863018 (A469S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140953	NM_018677.4(ACSS2):c.1430C>G (p.Pro477Arg)	ACSS2, LOC126863018 (P490R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363608	NM_018677.4(ACSS2):c.1441G>A (p.Ala481Thr)	ACSS2, LOC126863018 (A386T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605237	NM_018677.4(ACSS2):c.1448C>A (p.Pro483His)	ACSS2, LOC126863018 (P388H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600109	NM_018677.4(ACSS2):c.1459G>A (p.Gly487Ser)	ACSS2, LOC126863018 (G392S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480044	NM_018677.4(ACSS2):c.1505A>G (p.Asn502Ser)	ACSS2, LOC126863018 (N502S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614745	NM_018677.4(ACSS2):c.1519G>A (p.Glu507Lys)	ACSS2, LOC126863018 (E412K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346357	NM_018677.4(ACSS2):c.1534G>A (p.Ala512Thr)	ACSS2, LOC126863018 (A512T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance