ClinVar Miner

List of variants in gene POLK studied for cancer

Included ClinVar conditions (474):
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_016218.6(POLK):c.85G>A (p.Glu29Lys) rs148960463 0.00137
NM_016218.6(POLK):c.1284G>A (p.Ala428=) rs770984846 0.00001
NM_016218.6(POLK):c.*66T>C rs786205688
NM_016218.6(POLK):c.1256A>G (p.Glu419Gly) rs111584802
NM_016218.6(POLK):c.1289A>G (p.Glu430Gly) rs1554062741
NM_016218.6(POLK):c.1324C>T (p.Leu442Phe) rs1554062789
NM_016218.6(POLK):c.1341G>A (p.Gln447=) rs1554062804
NM_016218.6(POLK):c.1345G>A (p.Glu449Lys) rs1304454699
NM_016218.6(POLK):c.1381A>G (p.Lys461Glu) rs1554063600
NM_016218.6(POLK):c.1460T>C (p.Ile487Thr) rs1554063656
NM_016218.6(POLK):c.1582A>T (p.Ser528Cys) rs139591993
NM_016218.6(POLK):c.1652A>T (p.Asp551Val) rs1554064175
NM_016218.6(POLK):c.1692G>A (p.Lys564=) rs781194178
NM_016218.6(POLK):c.1741G>A (p.Asp581Asn) rs863225457
NM_016218.6(POLK):c.2033C>T (p.Ser678Phe) rs863225455
NM_016218.6(POLK):c.2192T>A (p.Leu731His) rs863225456
NM_016218.6(POLK):c.2598T>G (p.Asp866Glu) rs1554064740
NM_016218.6(POLK):c.410C>T (p.Ser137Phe) rs863225454
NM_016218.6(POLK):c.461G>A (p.Gly154Glu) rs749804502
NM_016218.6(POLK):c.464T>C (p.Phe155Ser) rs1554059550
NM_016218.6(POLK):c.512T>C (p.Phe171Ser) rs1554059573

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