"Ambry Genetics"[submitter] AND "SSR1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2243179	NM_003144.5(SSR1):c.644C>T (p.Ala215Val)	SSR1 (A147V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170485	NM_003144.5(SSR1):c.596G>C (p.Arg199Thr)	SSR1 (R131T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588289	NM_003144.5(SSR1):c.332G>A (p.Gly111Asp)	SSR1 (G111D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2257543	NM_003144.5(SSR1):c.253A>G (p.Thr85Ala)	SSR1 (T85A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3170484	NM_003144.5(SSR1):c.172G>A (p.Glu58Lys)	SSR1 (E58K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358241	NM_003144.5(SSR1):c.52A>G (p.Thr18Ala)	SSR1 (T18A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263112	NM_003144.5(SSR1):c.37C>G (p.Leu13Val)	SSR1 (L13V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar