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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2569647	NM_031210.6(SLIRP):c.16G>T (p.Ala6Ser)	SLIRP (A6S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351127	NM_031210.6(SLIRP):c.58G>C (p.Val20Leu)	SLIRP (V20L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3320481	NM_031210.6(SLIRP):c.127G>A (p.Gly43Ser)	SLIRP (G43S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346252	NM_031210.6(SLIRP):c.212A>G (p.Glu71Gly)	SLIRP (E71G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372522	NM_031210.6(SLIRP):c.230T>A (p.Leu77Gln)	SLIRP (L77Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353445	NM_031210.6(SLIRP):c.254A>G (p.Asp85Gly)	SLIRP (D85G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165999	NM_031210.6(SLIRP):c.320A>G (p.Lys107Arg)	SLIRP (K105R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar