"Ambry Genetics"[submitter] AND "LOC129998698"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2325673	NM_080744.2(SSC4D):c.1295A>G (p.Asn432Ser)	LOC129998698, SSC4D (N432S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284021	NM_080744.2(SSC4D):c.1273C>T (p.His425Tyr)	LOC129998698, SSC4D (H425Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409995	NM_080744.2(SSC4D):c.1153G>A (p.Ala385Thr)	LOC129998698, SSC4D (A385T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338019	NM_080744.2(SSC4D):c.1067G>A (p.Arg356His)	LOC129998698, SSC4D (R356H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328599	NM_080744.2(SSC4D):c.1063G>C (p.Gly355Arg)	LOC129998698, SSC4D (G355R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607566	NM_080744.2(SSC4D):c.1061G>C (p.Arg354Pro)	LOC129998698, SSC4D (R354P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400984	NM_080744.2(SSC4D):c.1023T>G (p.Ser341Arg)	LOC129998698, SSC4D (S341R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343986	NM_080744.2(SSC4D):c.1001C>T (p.Ala334Val)	LOC129998698, SSC4D (A334V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245150	NM_080744.2(SSC4D):c.1000G>A (p.Ala334Thr)	LOC129998698, SSC4D (A334T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance