List of variants in gene RPGRIP1L reported by OMIM

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_015272.5(RPGRIP1L):c.685G>A (p.Ala229Thr)	rs61747071	0.04969
NM_015272.5(RPGRIP1L):c.2614C>T (p.Gln872Ter)	rs121918203	0.00005
NM_015272.5(RPGRIP1L):c.1843A>C (p.Thr615Pro)	rs121918198	0.00004
NM_015272.5(RPGRIP1L):c.697A>T (p.Lys233Ter)	rs121918197	0.00004
NM_015272.5(RPGRIP1L):c.2050C>T (p.Gln684Ter)	rs121918204	0.00002
NM_015272.5(RPGRIP1L):c.2413C>T (p.Arg805Ter)	rs145665129	0.00001
NM_015272.5(RPGRIP1L):c.1033C>T (p.Gln345Ter)	rs121918202
NM_015272.5(RPGRIP1L):c.1721del (p.Tyr574fs)	rs863225216
NM_015272.5(RPGRIP1L):c.1975T>C (p.Ser659Pro)	rs267607020
NM_015272.5(RPGRIP1L):c.2083G>C (p.Ala695Pro)	rs121918200
NM_015272.5(RPGRIP1L):c.2269del (p.Thr757fs)	rs387906243
NM_015272.5(RPGRIP1L):c.394A>T (p.Arg132Ter)	rs121918201
NM_015272.5(RPGRIP1L):c.757C>T (p.Gln253Ter)	rs121918199

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