ClinVar Miner

List of variants in gene PCLO reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_033026.6(PCLO):c.5632A>G (p.Ile1878Val) rs150515688 0.00262
NM_033026.6(PCLO):c.962A>G (p.His321Arg) rs139392690 0.00223
NM_033026.6(PCLO):c.10767C>G (p.Asp3589Glu) rs149879954 0.00221
NM_033026.6(PCLO):c.775C>G (p.Gln259Glu) rs10251512 0.00220
NM_033026.6(PCLO):c.1297G>A (p.Ala433Thr) rs201344475 0.00180
NM_033026.6(PCLO):c.14702A>G (p.Lys4901Arg) rs149360770 0.00127
NM_033026.6(PCLO):c.3862G>T (p.Gly1288Trp) rs199689461 0.00081
NM_033026.6(PCLO):c.12058A>G (p.Ser4020Gly) rs201095081 0.00058
NM_033026.6(PCLO):c.14999A>G (p.Asp5000Gly) rs569988068 0.00045
NM_033026.6(PCLO):c.6167G>A (p.Arg2056Lys) rs189561105 0.00029
NM_033026.6(PCLO):c.212T>C (p.Val71Ala) rs370728784 0.00026
NM_033026.6(PCLO):c.7585A>G (p.Ile2529Val) rs574590559 0.00021
NM_033026.6(PCLO):c.6269A>T (p.Asp2090Val) rs143208658 0.00018
NM_033026.6(PCLO):c.7162G>A (p.Ala2388Thr) rs372868247 0.00017
NM_033026.6(PCLO):c.1148C>T (p.Ser383Leu) rs767073368 0.00008
NM_033026.6(PCLO):c.11332G>A (p.Ala3778Thr) rs374145934 0.00006
NM_033026.6(PCLO):c.8662G>A (p.Val2888Ile) rs529385259 0.00006
NM_033026.6(PCLO):c.12950A>G (p.Lys4317Arg) rs751802785 0.00002
NM_033026.6(PCLO):c.14035G>A (p.Gly4679Ser) rs780079111 0.00002
NM_033026.6(PCLO):c.2212C>A (p.Pro738Thr) rs191183215 0.00001
NM_033026.6(PCLO):c.3863G>A (p.Gly1288Glu) rs370173546 0.00001
NM_033026.6(PCLO):c.8347T>C (p.Ser2783Pro) rs201921094 0.00001
NM_033026.6(PCLO):c.15168G>A (p.Met5056Ile)
NM_033026.6(PCLO):c.1531C>T (p.Pro511Ser)
NM_033026.6(PCLO):c.2674C>T (p.Pro892Ser)
NM_033026.6(PCLO):c.3230A>G (p.Asn1077Ser)
NM_033026.6(PCLO):c.3518T>C (p.Leu1173Pro) rs761053170
NM_033026.6(PCLO):c.3539T>C (p.Leu1180Pro)
NM_033026.6(PCLO):c.4424G>A (p.Arg1475Lys)
NM_033026.6(PCLO):c.6746G>A (p.Arg2249Gln)
NM_033026.6(PCLO):c.79A>G (p.Ser27Gly)
NM_033026.6(PCLO):c.9015T>G (p.Phe3005Leu)

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