"PreventionGenetics, part of Exact Sciences"[submitter] AND "ABCC1"[ge - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049946	NM_004996.4(ABCC1):c.185G>A (p.Arg62Gln)	ABCC1 (R62Q)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GBenign
Select item 3053129	NM_004996.4(ABCC1):c.275C>T (p.Ser92Phe)	ABCC1 (S92F)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GBenign
Select item 3034993	NM_004996.4(ABCC1):c.854C>T (p.Pro285Leu)	ABCC1 (P285L)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GLikely benign
Select item 3046554	NM_004996.4(ABCC1):c.1235A>G (p.Asn412Ser)	ABCC1 (N412S)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GLikely benign
Select item 3041981	NM_004996.4(ABCC1):c.1898G>A (p.Arg633Gln)	ABCC1 (R633Q)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GLikely benign
Select item 779968	NM_004996.4(ABCC1):c.1911C>T (p.Asp637=)	ABCC1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3036882	NM_004996.4(ABCC1):c.1915G>T (p.Gly639Trp)	ABCC1 (G639W)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GLikely benign
Select item 3054117	NM_004996.4(ABCC1):c.3019G>A (p.Gly1007Arg)	ABCC1 (G1007R +1 more)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GBenign
Select item 3033652	NM_004996.4(ABCC1):c.3308G>A (p.Gly1103Asp)	ABCC1 (G1044D +1 more)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GLikely benign
Select item 3035903	NM_004996.4(ABCC1):c.3346G>A (p.Ala1116Thr)	ABCC1 (A1057T +1 more)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GLikely benign
Select item 3041865	NM_004996.4(ABCC1):c.4202C>T (p.Thr1401Met)	ABCC1 (T1342M +1 more)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GLikely benign
Select item 3046258	NM_004996.4(ABCC1):c.4441G>A (p.Val1481Ile)	ABCC1 (V1422I +1 more)	Single nucleotide variant (missense variant)	ABCC1-related disorder	GBenign