"Ambry Genetics"[submitter] AND "LOC129992330"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1338950	NM_016955.4(SEPSECS):c.94A>G (p.Ile32Val)	LOC129992330, SEPSECS (I32V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2223555	NM_016955.4(SEPSECS):c.83A>G (p.His28Arg)	LOC129992330, SEPSECS (H28R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance