"Ambry Genetics"[submitter] AND "LOC126862498"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3155867	NM_005963.4(MYH1):c.4880A>G (p.Asn1627Ser)	LOC126862498, MYH1 +1 more (N1627S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371287	NM_005963.4(MYH1):c.4780C>A (p.His1594Asn)	LOC126862498, MYH1 +1 more (H1594N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155862	NM_005963.4(MYH1):c.4768A>C (p.Met1590Leu)	LOC126862498, MYH1 +1 more (M1590L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2232606	NM_005963.4(MYH1):c.4754A>G (p.Glu1585Gly)	LOC126862498, MYH1 +1 more (E1585G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210197	NM_005963.4(MYH1):c.4733G>A (p.Arg1578Lys)	LOC126862498, MYH1 +1 more (R1578K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331347	NM_005963.4(MYH1):c.4616A>G (p.Gln1539Arg)	LOC126862498, MYH1 +1 more (Q1539R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368142	NM_005963.4(MYH1):c.4586A>C (p.Glu1529Ala)	LOC126862498, MYH1 +1 more (E1529A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155850	NM_005963.4(MYH1):c.4576C>T (p.Arg1526Cys)	LOC126862498, MYH1 +1 more (R1526C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493939	NM_005963.4(MYH1):c.4547T>C (p.Leu1516Pro)	LOC126862498, MYH1 +1 more (L1516P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155845	NM_005963.4(MYH1):c.4507A>C (p.Lys1503Gln)	LOC126862498, MYH1 +1 more (K1503Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373123	NM_005963.4(MYH1):c.4435C>T (p.Arg1479Cys)	LOC126862498, MYH1 +1 more (R1479C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155826	NM_005963.4(MYH1):c.4406C>G (p.Ala1469Gly)	LOC126862498, MYH1 +1 more (A1469G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance