"Eurofins Ntd Llc (ga)"[submitter] AND "RP9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 198295	NM_203288.2(RP9):c.664del (p.Ter222AspextTer?)	RP9	Deletion (frameshift variant +1 more)	Retinitis pigmentosa 9 +3 more	GBenign/Likely benign
Select item 167609	NM_203288.2(RP9):c.629A>G (p.Lys210Arg)	RP9 (K210R)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +3 more	GBenign
Select item 167610	NM_203288.2(RP9):c.463G>A (p.Val155Ile)	RP9 (V155I)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +2 more	GBenign
Select item 167611	NM_203288.2(RP9):c.459G>A (p.Lys153=)	RP9	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 593532	NM_203288.2(RP9):c.290G>A (p.Gly97Glu)	RP9 (G97E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 196604	NM_203288.2(RP9):c.216A>G (p.Pro72=)	RP9	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 193521	NM_203288.2(RP9):c.34G>A (p.Ala12Thr)	LOC129998225, RP9 (A12T)	Single nucleotide variant (missense variant)	Retinitis pigmentosa +1 more	GConflicting classifications of pathogenicity

ClinVar