ClinVar Miner

List of variants in gene PCCB reported as benign for not provided

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000532.5(PCCB):c.1498+278A>G rs483465 0.75970
NM_000532.4(PCCB):c.-390G>C rs3755636 0.75389
NM_000532.5(PCCB):c.1090+320A>G rs1291921 0.72973
NM_000532.5(PCCB):c.967-46A>G rs9833162 0.36992
NM_000532.5(PCCB):c.764-316A>G rs56336182 0.17162
NM_000532.5(PCCB):c.654+20T>C rs3821445 0.15527
NM_000532.5(PCCB):c.373-1009G>A rs76931214 0.02335
NM_000532.5(PCCB):c.1398+238C>T rs78209731 0.01783
NM_000532.5(PCCB):c.763+244A>G rs76321585 0.01769
NM_000532.5(PCCB):c.546G>A (p.Arg182=) rs61598773 0.00533
NM_000532.5(PCCB):c.372+31T>C rs16843829 0.00526
NM_000532.5(PCCB):c.1499-48A>G rs144001285 0.00234
NM_000532.5(PCCB):c.184-12G>T rs181283691 0.00185
NM_000532.5(PCCB):c.1490C>T (p.Ala497Val) rs142403318 0.00162
NM_000532.5(PCCB):c.654+3A>C rs199886085 0.00014
NM_000532.5(PCCB):c.1090+172_1090+178del rs397694948
NM_000532.5(PCCB):c.1090+174_1090+178dup rs397694948
NM_000532.5(PCCB):c.1090+175_1090+178dup rs397694948
NM_000532.5(PCCB):c.1090+178dup rs397694948
NM_000532.5(PCCB):c.430-121C>G rs2290131
NM_000532.5(PCCB):c.654+369_654+370insGA rs59010681
NM_000532.5(PCCB):c.654+370_654+371insGTTTCA rs67922183
NM_000532.5(PCCB):c.654+405A>C rs16843879

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