ClinVar Miner

List of variants in gene RPGRIP1L reported as likely benign for not provided

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Gene type:
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Total variants: 65
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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.3790G>A (p.Asp1264Asn) rs3213758 0.04663
NM_015272.5(RPGRIP1L):c.1581+162G>C rs72803648 0.02744
NM_015272.5(RPGRIP1L):c.2231G>A (p.Arg744Gln) rs2302677 0.02738
NM_015272.5(RPGRIP1L):c.3701+90G>A rs147132440 0.01848
NM_015272.5(RPGRIP1L):c.2959-15T>C rs11863101 0.01368
NM_015272.5(RPGRIP1L):c.632+258G>A rs146320462 0.01223
NM_015272.5(RPGRIP1L):c.3616+77G>A rs74018105 0.01115
NM_015272.5(RPGRIP1L):c.632+291G>A rs142351387 0.00960
NM_015272.5(RPGRIP1L):c.776+89T>C rs72803655 0.00885
NM_015272.5(RPGRIP1L):c.3548C>G (p.Ala1183Gly) rs139974543 0.00854
NM_015272.5(RPGRIP1L):c.3835+323C>T rs11862484 0.00787
NM_015272.5(RPGRIP1L):c.3372C>T (p.Ser1124=) rs146902870 0.00702
NM_015272.5(RPGRIP1L):c.1244-78G>A rs115739140 0.00699
NM_015272.5(RPGRIP1L):c.2304+304T>C rs189252764 0.00699
NM_015272.5(RPGRIP1L):c.883-198T>C rs138067503 0.00691
NM_015272.5(RPGRIP1L):c.2153-110C>T rs11859403 0.00581
NM_015272.5(RPGRIP1L):c.3221-38T>C rs11860764 0.00566
NM_015272.5(RPGRIP1L):c.*491C>G rs35669682 0.00564
NM_015272.5(RPGRIP1L):c.2152+171A>G rs140672076 0.00555
NM_015272.5(RPGRIP1L):c.2925A>G (p.Val975=) rs144313291 0.00524
NM_015272.5(RPGRIP1L):c.*1627G>A rs188203905 0.00522
NM_015272.5(RPGRIP1L):c.1165A>G (p.Ile389Val) rs79708859 0.00517
NM_015272.5(RPGRIP1L):c.1582-305A>C rs111274730 0.00475
NM_015272.5(RPGRIP1L):c.882+140T>C rs189766524 0.00406
NM_015272.5(RPGRIP1L):c.1244-173T>A rs149754212 0.00347
NM_015272.5(RPGRIP1L):c.2304+285G>A rs192285320 0.00346
NM_015272.5(RPGRIP1L):c.1340T>C (p.Leu447Ser) rs138155747 0.00322
NM_015272.5(RPGRIP1L):c.3745G>T (p.Asp1249Tyr) rs148773489 0.00266
NM_015272.5(RPGRIP1L):c.532A>G (p.Ile178Val) rs140067659 0.00245
NM_015272.5(RPGRIP1L):c.2807T>G (p.Ile936Ser) rs146197239 0.00244
NM_015272.5(RPGRIP1L):c.883-50A>C rs140246925 0.00244
NM_015272.5(RPGRIP1L):c.530-51C>A rs148326584 0.00221
NM_015272.5(RPGRIP1L):c.777-290A>T rs79980281 0.00204
NM_015272.5(RPGRIP1L):c.2673G>A (p.Arg891=) rs61742381 0.00195
NM_015272.5(RPGRIP1L):c.1030-50A>C rs201831442 0.00185
NM_015272.5(RPGRIP1L):c.2643T>A (p.Asn881Lys) rs139503476 0.00157
NM_015272.5(RPGRIP1L):c.2153-4G>C rs201380599 0.00156
NM_015272.5(RPGRIP1L):c.640G>A (p.Val214Ile) rs139067427 0.00146
NM_015272.5(RPGRIP1L):c.482G>A (p.Arg161His) rs74957591 0.00118
NM_015272.5(RPGRIP1L):c.-7-38T>C rs148157252 0.00102
NM_015272.5(RPGRIP1L):c.1072T>C (p.Leu358=) rs147295026 0.00101
NM_015272.5(RPGRIP1L):c.1660C>A (p.Leu554Ile) rs79524027 0.00092
NM_015272.5(RPGRIP1L):c.2240G>A (p.Arg747Gln) rs142349647 0.00085
NM_015272.5(RPGRIP1L):c.3300C>T (p.Leu1100=) rs190706759 0.00077
NM_015272.5(RPGRIP1L):c.2684-40C>T rs117194361 0.00065
NM_015272.5(RPGRIP1L):c.3624C>T (p.Tyr1208=) rs138724933 0.00063
NM_015272.5(RPGRIP1L):c.*1584G>T rs151226475 0.00057
NM_015272.5(RPGRIP1L):c.3312C>T (p.Pro1104=) rs568801926 0.00046
NM_015272.5(RPGRIP1L):c.231-33A>G rs189750129 0.00033
NM_015272.5(RPGRIP1L):c.2682A>G (p.Ser894=) rs141608712 0.00033
NM_015272.5(RPGRIP1L):c.1704A>G (p.Gln568=) rs141201084 0.00014
NM_015272.5(RPGRIP1L):c.530-15T>C rs368728064 0.00014
NM_015272.5(RPGRIP1L):c.1872T>C (p.Ser624=) rs149464542 0.00006
NM_015272.5(RPGRIP1L):c.3331G>A (p.Ala1111Thr) rs973841786 0.00003
NM_015272.5(RPGRIP1L):c.529+17G>A rs754295905 0.00003
NM_015272.5(RPGRIP1L):c.1944G>A (p.Val648=) rs532450170 0.00001
NM_015272.5(RPGRIP1L):c.1104-247del rs376487101
NM_015272.5(RPGRIP1L):c.1581+194dup rs991639713
NM_015272.5(RPGRIP1L):c.1701C>A (p.Ala567=) rs1555604462
NM_015272.5(RPGRIP1L):c.1770T>G (p.Ser590=) rs966605945
NM_015272.5(RPGRIP1L):c.2049C>T (p.His683=) rs1450344678
NM_015272.5(RPGRIP1L):c.3295-8del rs113083177
NM_015272.5(RPGRIP1L):c.3555G>A (p.Glu1185=) rs2150964438
NM_015272.5(RPGRIP1L):c.883-32_883-30del rs201808974

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