"Ambry Genetics"[submitter] AND "LOC129937260"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3102156	NM_017577.5(GRAMD1C):c.14C>G (p.Pro5Arg)	GRAMD1C, LOC129937260 (P5R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361488	NM_017577.5(GRAMD1C):c.14C>T (p.Pro5Leu)	GRAMD1C, LOC129937260 (P5L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2204364	NM_017577.5(GRAMD1C):c.22C>A (p.Arg8Ser)	GRAMD1C, LOC129937260 (R8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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