ClinVar Miner

List of variants in gene PCCB reported as likely benign for not specified

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_000532.5(PCCB):c.49C>A (p.Leu17Met) rs200185747 0.00172
NM_000532.5(PCCB):c.774C>G (p.His258Gln) rs141615209 0.00163
NM_000532.5(PCCB):c.138G>C (p.Ala46=) rs145075817 0.00126
NM_000532.5(PCCB):c.882C>T (p.Pro294=) rs142730126 0.00080
NM_000532.5(PCCB):c.429+7G>A rs201986472 0.00073
NM_000532.5(PCCB):c.544-20T>C rs370010917 0.00011
NM_000532.5(PCCB):c.373-18T>C rs775972133 0.00009
NM_000532.5(PCCB):c.1569C>G (p.Ala523=) rs1418405958 0.00003
NM_000532.5(PCCB):c.372+15C>T rs370726053 0.00003
NM_000532.5(PCCB):c.24G>T (p.Ala8=) rs1057523611 0.00002
NM_000532.5(PCCB):c.348A>G (p.Gly116=) rs1057522223 0.00001
NM_000532.5(PCCB):c.747C>T (p.Thr249=) rs746448544 0.00001
NM_000532.5(PCCB):c.-12G>A rs1553773141
NM_000532.5(PCCB):c.1090+4G>A rs1553782783
NM_000532.5(PCCB):c.1452A>G (p.Ala484=) rs781556055
NM_000532.5(PCCB):c.303+19_303+21del rs1338554743
NM_000532.5(PCCB):c.304-16dup rs555567135
NM_000532.5(PCCB):c.654+465T>C rs1332518948
NM_000532.5(PCCB):c.764-19A>G rs779517974
NM_000532.5(PCCB):c.885-18C>T rs1482092717
NM_000532.5(PCCB):c.9G>C (p.Ala3=) rs763025114

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