"Baylor Genetics"[submitter] AND "LOC126807437"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 657862	NM_002439.5(MSH3):c.923A>T (p.Lys308Met)	LOC126807437, MSH3 (K308M)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 657947	NM_002439.5(MSH3):c.953T>C (p.Ile318Thr)	LOC126807437, MSH3 (I318T)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 657893	NM_002439.5(MSH3):c.978_984del (p.Phe326fs)	MSH3, LOC126807437 (F326fs)	Deletion (frameshift variant)	Familial adenomatous polyposis 4 +3 more	GPathogenic/Likely pathogenic
Select item 655120	NM_002439.5(MSH3):c.982C>T (p.Arg328Trp)	LOC126807437, MSH3 (R328W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 823502	NM_002439.5(MSH3):c.983G>A (p.Arg328Gln)	LOC126807437, MSH3 (R328Q)	Single nucleotide variant (missense variant)	Endometrial carcinoma +2 more	GUncertain significance
Select item 1754952	NM_002439.5(MSH3):c.1000T>C (p.Tyr334His)	LOC126807437, MSH3 (Y334H)	Single nucleotide variant (missense variant)	Endometrial carcinoma +2 more	GUncertain significance
Select item 645316	NM_002439.5(MSH3):c.1001A>T (p.Tyr334Phe)	MSH3, LOC126807437 (Y334F)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2020610	NM_002439.5(MSH3):c.1017_1018insC (p.Ile340fs)	LOC126807437, MSH3 (I340fs)	Insertion (frameshift variant)	Familial adenomatous polyposis 4 +2 more	GPathogenic/Likely pathogenic
Select item 652629	NM_002439.5(MSH3):c.1019T>C (p.Ile340Thr)	LOC126807437, MSH3 (I340T)	Single nucleotide variant (missense variant)	Endometrial carcinoma +2 more	GUncertain significance