ClinVar Miner

List of variants in gene RPGR reported as not provided by Retina International

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Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP gnomAD frequency
NM_001034853.2(RPGR):c.1245+16A>G rs5918522 0.13807
NM_001034853.2(RPGR):c.1164G>A (p.Ala388=) rs1801686 0.11812
NM_001034853.2(RPGR):c.1697G>A (p.Gly566Glu) rs1801688 0.09526
NM_001034853.2(RPGR):c.1572+11A>G rs62635008 0.09352
NM_001034853.2(RPGR):c.1507-97T>C rs62635007 0.09306
NM_001034853.2(RPGR):c.1274G>A (p.Arg425Lys) rs1801687 0.09261
NM_001034853.2(RPGR):c.1291A>G (p.Ile431Val) rs62635003 0.05955
NM_001034853.2(RPGR):c.620-41T>C rs45486397 0.03373
NM_001034853.2(RPGR):c.1598C>T (p.Thr533Met) rs41312104 0.02014
NM_001034853.2(RPGR):c.1033A>G (p.Asn345Asp) rs41305223 0.00731
NM_001034853.2(RPGR):c.732G>A (p.Lys244=) rs62638654 0.00191
NM_001034853.2(RPGR):c.141T>G (p.Ser47=) rs62638631 0.00034
NM_001034853.2(RPGR):c.865A>G (p.Ile289Val) rs62640587 0.00005
NM_001034853.2(RPGR):c.106G>T (p.Val36Phe) rs62638628 0.00001
NM_001034853.2(RPGR):c.778+5G>A rs62640583 0.00001
NM_000328.2(RPGR):c.*477_*497dup rs281865320
NM_000328.2(RPGR):c.*624_*635del rs281865321
NM_000328.2(RPGR):c.*638_*649del rs281865322
NM_000328.2(RPGR):c.*874_*875insA rs281865323
NM_000328.3(RPGR):c.*158_*172del rs281865317
NM_000328.3(RPGR):c.*177dup rs281865318
NM_000328.3(RPGR):c.*372_*392dup rs281865319
NM_000328.3(RPGR):c.*76del rs281865315
NM_000328.3(RPGR):c.*94_*114del rs281865316
NM_000328.3(RPGR):c.2055A>G (p.Arg685=) rs281865306
NM_000328.3(RPGR):c.2080A>T (p.Thr694Ser) rs281865307
NM_000328.3(RPGR):c.2226G>A (p.Met742Ile) rs281865308
NM_000328.3(RPGR):c.2259A>T (p.Arg753Ser) rs281865309
NM_000328.3(RPGR):c.2260G>T (p.Val754Phe) rs281865310
NM_000328.3(RPGR):c.2311del (p.Glu771fs) rs281865311
NM_000328.3(RPGR):c.2357_2358del (p.Lys786fs) rs281865312
NM_000328.3(RPGR):c.2357_2375del (p.Lys786fs) rs281865313
NM_000328.3(RPGR):c.2447_*13del (p.Ter816Xaa) rs281865314
NM_001034853.2(RPGR):c.101del (p.Asn34fs) rs281865295
NM_001034853.2(RPGR):c.1092dup (p.Ala365fs) rs281865301
NM_001034853.2(RPGR):c.1100del (p.Pro367fs) rs62635000
NM_001034853.2(RPGR):c.1120G>T (p.Glu374Ter) rs62635001
NM_001034853.2(RPGR):c.1243_1244dup (p.Glu416fs) rs281865302
NM_001034853.2(RPGR):c.1245+3A>G rs62635002
NM_001034853.2(RPGR):c.1261_1279del (p.Ser421fs) rs281865303
NM_001034853.2(RPGR):c.127G>A (p.Gly43Arg) rs62638629
NM_001034853.2(RPGR):c.128G>A (p.Gly43Glu) rs62638630
NM_001034853.2(RPGR):c.1307G>A (p.Gly436Asp) rs62635004
NM_001034853.2(RPGR):c.1377_1378del (p.Leu460fs) rs62653029
NM_001034853.2(RPGR):c.1402_1405del (p.Pro468fs) rs62653030
NM_001034853.2(RPGR):c.1477del (p.Gly494fs) rs62635005
NM_001034853.2(RPGR):c.1478T>A (p.Leu493His) rs62635006
NM_001034853.2(RPGR):c.1507-68T>C rs62643066
NM_001034853.2(RPGR):c.1512_1513del (p.Ile505fs) rs281865304
NM_001034853.2(RPGR):c.154G>T (p.Gly52Ter) rs281865296
NM_001034853.2(RPGR):c.155-2A>G rs62638632
NM_001034853.2(RPGR):c.1573-1G>A rs62635010
NM_001034853.2(RPGR):c.1573-2A>G rs62635009
NM_001034853.2(RPGR):c.1573-8A>G rs62635011
NM_001034853.2(RPGR):c.1575_1578del (p.Lys525fs) rs281865305
NM_001034853.2(RPGR):c.1576CAA[1] (p.Gln527del) rs62653033
NM_001034853.2(RPGR):c.1747G>T (p.Glu583Ter) rs62635013
NM_001034853.2(RPGR):c.179G>T (p.Gly60Val) rs62638634
NM_001034853.2(RPGR):c.1835dup (p.Asn612fs) rs62635014
NM_001034853.2(RPGR):c.237_238del (p.Val81fs) rs62650215
NM_001034853.2(RPGR):c.248-2A>G rs62638633
NM_001034853.2(RPGR):c.248-6T>A rs62638635
NM_001034853.2(RPGR):c.294C>A (p.His98Gln) rs62638636
NM_001034853.2(RPGR):c.295_296dup (p.Leu100fs) rs62638638
NM_001034853.2(RPGR):c.296C>A (p.Thr99Asn) rs62638637
NM_001034853.2(RPGR):c.310+1G>C rs62638639
NM_001034853.2(RPGR):c.310+3A>G rs62638640
NM_001034853.2(RPGR):c.356del (p.Leu119fs) rs62638641
NM_001034853.2(RPGR):c.372del (p.Glu125fs) rs62638642
NM_001034853.2(RPGR):c.379A>G (p.Arg127Gly) rs62638643
NM_001034853.2(RPGR):c.389T>G (p.Phe130Cys) rs62638644
NM_001034853.2(RPGR):c.415G>T (p.Glu139Ter) rs62638645
NM_001034853.2(RPGR):c.469+1G>A rs62638646
NM_001034853.2(RPGR):c.485_486del (p.Phe162fs) rs281865297
NM_001034853.2(RPGR):c.486del (p.Phe162fs) rs281865297
NM_001034853.2(RPGR):c.492G>A (p.Trp164Ter) rs62638648
NM_001034853.2(RPGR):c.581G>A (p.Trp194Ter) rs62650216
NM_001034853.2(RPGR):c.605C>A (p.Ser202Ter) rs62650217
NM_001034853.2(RPGR):c.619+5G>A rs62638649
NM_001034853.2(RPGR):c.644G>T (p.Gly215Val) rs62650218
NM_001034853.2(RPGR):c.703C>T (p.Pro235Ser) rs62638651
NM_001034853.2(RPGR):c.706C>T (p.Gln236Ter) rs62638652
NM_001034853.2(RPGR):c.730A>T (p.Lys244Ter) rs62638653
NM_001034853.2(RPGR):c.747del (p.Cys250fs) rs62650219
NM_001034853.2(RPGR):c.748T>C (p.Cys250Arg) rs62650220
NM_001034853.2(RPGR):c.750_751del (p.Cys250fs) rs281865299
NM_001034853.2(RPGR):c.779-1G>A rs62638655
NM_001034853.2(RPGR):c.823G>A (p.Gly275Ser) rs62642057
NM_001034853.2(RPGR):c.833_836del (p.Thr278fs) rs62640584
NM_001034853.2(RPGR):c.836_837del (p.Phe279fs) rs62640586
NM_001034853.2(RPGR):c.837del (p.Leu280fs) rs62640586
NM_001034853.2(RPGR):c.869del (p.Glu290fs) rs62640588
NM_001034853.2(RPGR):c.886_900del (p.Thr296_Ile300del) rs62653026
NM_001034853.2(RPGR):c.904T>C (p.Cys302Arg) rs62640589
NM_001034853.2(RPGR):c.905G>A (p.Cys302Tyr) rs62640590
NM_001034853.2(RPGR):c.931A>G (p.Thr311Ala) rs62640591
NM_001034853.2(RPGR):c.934+1G>A rs62640592
NM_001034853.2(RPGR):c.934+1G>C rs62640592
NM_001034853.2(RPGR):c.958G>A (p.Gly320Arg) rs62640593
NM_001034853.2(RPGR):c.980T>G (p.Leu327Ter) rs62640594
NM_001034853.2(RPGR):c.994G>T (p.Glu332Ter) rs62642058

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