List of variants in gene RPGRIP1 reported by Clinical Genetics, Academic Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.1639G>T (p.Ala547Ser)	rs10151259	0.21790
NM_020366.4(RPGRIP1):c.3341A>G (p.Asp1114Gly)	rs17103671	0.02649
NM_020366.4(RPGRIP1):c.2284C>T (p.Leu762=)	rs145896974	0.00240
NM_020366.4(RPGRIP1):c.1753C>T (p.Pro585Ser)	rs147586703	0.00155
NM_020366.4(RPGRIP1):c.95T>A (p.Met32Lys)	rs200510462	0.00140
NM_020366.4(RPGRIP1):c.450C>G (p.Leu150=)	rs144585562	0.00130
NM_020366.4(RPGRIP1):c.3171C>T (p.His1057=)	rs201838837	0.00053
NM_020366.4(RPGRIP1):c.3358A>G (p.Ile1120Val)	rs137853911	0.00051
NM_020366.4(RPGRIP1):c.2711-13G>T	rs369991630	0.00026
NM_020366.4(RPGRIP1):c.491-3T>C	rs749376395	0.00011
NM_020366.4(RPGRIP1):c.2397C>T (p.Asn799=)	rs375546482	0.00006
NM_020366.4(RPGRIP1):c.2554C>T (p.Arg852Ter)	rs1429786931	0.00001
NM_020366.4(RPGRIP1):c.1948C>T (p.Pro650Ser)	rs1740380459

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