ClinVar Miner

List of variants in gene CYGB, PRCD studied for Retinitis pigmentosa

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001077620.3(PRCD):c.*1397A>G rs4232870 0.47066
NM_001077620.3(PRCD):c.*1405C>T rs4648339 0.27446
NM_001077620.3(PRCD):c.*760C>T rs2278639 0.25158
NM_001077620.3(PRCD):c.*1439T>C rs5742903 0.22457
NM_001077620.3(PRCD):c.*1185A>C rs895157 0.19185
NM_001077620.3(PRCD):c.*933G>A rs73998961 0.03370
NM_001077620.3(PRCD):c.74+14C>T rs200645008 0.00674
NM_001077620.3(PRCD):c.*1259G>A rs144852411 0.00616
NM_001077620.3(PRCD):c.*1186G>A rs568033840 0.00609
NM_001077620.3(PRCD):c.*1618C>T rs77404579 0.00535
NM_001077620.3(PRCD):c.*1097T>A rs76768775 0.00488
NM_001077620.3(PRCD):c.*266C>T rs72860161 0.00403
NM_001077620.3(PRCD):c.*1650T>C rs185494982 0.00306
NM_001077620.3(PRCD):c.*1238G>A rs189599263 0.00292
NM_001077620.3(PRCD):c.*1480C>G rs139602114 0.00286
NM_001077620.3(PRCD):c.*1508C>T rs181845864 0.00200
NM_001077620.3(PRCD):c.*265C>T rs541445094 0.00151
NM_001077620.3(PRCD):c.*932C>T rs117784164 0.00068
NM_001077620.3(PRCD):c.*115G>A rs758393407 0.00038
NM_001077620.3(PRCD):c.*477C>T rs965177016 0.00034
NM_001077620.3(PRCD):c.*1347C>T rs780340686 0.00022
NM_001077620.3(PRCD):c.-82T>C rs1011242073 0.00015
NM_001077620.3(PRCD):c.*881G>A rs757028440 0.00014
NM_001077620.3(PRCD):c.*687G>A rs550804575 0.00012
NM_001077620.3(PRCD):c.13C>G (p.Leu5Val) rs200954045 0.00012
NM_001077620.3(PRCD):c.*260C>T rs773379904 0.00010
NM_001077620.3(PRCD):c.75-3C>G rs200091367 0.00006
NM_001077620.3(PRCD):c.*1343C>T rs886053481 0.00005
NM_001077620.3(PRCD):c.*1410G>C rs374415732 0.00005
NM_001077620.3(PRCD):c.*1188C>T rs887925408 0.00004
NM_001077620.3(PRCD):c.*749C>T rs776196684 0.00004
NM_001077620.3(PRCD):c.*907G>A rs750306157 0.00004
NM_001077620.3(PRCD):c.-94G>A rs892886625 0.00004
NM_001077620.3(PRCD):c.*1010G>A rs971307074 0.00003
NM_001077620.3(PRCD):c.*578C>G rs756335948 0.00003
NM_001077620.3(PRCD):c.*1061C>T rs552803584 0.00002
NM_001077620.3(PRCD):c.*1411G>A rs773610638 0.00002
NM_001077620.3(PRCD):c.64C>T (p.Arg22Ter) rs387907268 0.00002
NM_001077620.3(PRCD):c.*1509G>A rs777248455 0.00001
NM_001077620.3(PRCD):c.*413A>G rs775233504 0.00001
NM_001077620.3(PRCD):c.*605G>A rs886053477 0.00001
NM_001077620.3(PRCD):c.*764C>T rs886053479 0.00001
NM_001077620.3(PRCD):c.49C>T (p.Arg17Cys) rs375181336 0.00001
NM_001077620.3(PRCD):c.74+1G>A rs779066277 0.00001
NM_001077620.3(PRCD):c.*1002G>A rs1229301103
NM_001077620.3(PRCD):c.*1247C>A rs886053480
NM_001077620.3(PRCD):c.*1268C>A rs572748485
NM_001077620.3(PRCD):c.*1714C>T rs886053482
NM_001077620.3(PRCD):c.*241G>A rs1361539486
NM_001077620.3(PRCD):c.*248A>G rs886053475
NM_001077620.3(PRCD):c.*590C>A rs144319284
NM_001077620.3(PRCD):c.*643C>T rs745814897
NM_001077620.3(PRCD):c.102_111dup (p.Ser38Ter)
NM_001077620.3(PRCD):c.114C>T (p.Ser38=) rs2074979029
NM_001077620.3(PRCD):c.2T>C (p.Met1Thr) rs527236092
NM_001077620.3(PRCD):c.73C>A (p.Pro25Thr) rs2074970792
NM_001077620.3(PRCD):c.75-10C>A rs886053474
NM_001077620.3(PRCD):c.85G>C (p.Asp29His) rs372084413

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