ClinVar Miner

List of variants in gene PCCA 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
NM_000282.4(PCCA):c.105+273G>A rs7984311
NM_000282.4(PCCA):c.1745C>T (p.Ser582Leu) rs16957356
NM_000282.4(PCCA):c.1746+98T>A rs10508043
NM_000282.4(PCCA):c.1747-113G>A rs62619988
NM_000282.4(PCCA):c.1747-161C>T rs75527610
NM_000282.4(PCCA):c.184-305T>C rs4772265
NM_000282.4(PCCA):c.1846-104C>G rs1283292
NM_000282.4(PCCA):c.2040+172C>T rs837286
NM_000282.4(PCCA):c.2040+242G>T rs61614293
NM_000282.4(PCCA):c.2118+191G>C rs837335
NM_000282.4(PCCA):c.2119-204A>G rs857294
NM_000282.4(PCCA):c.300+300T>C rs73570922
NM_000282.4(PCCA):c.414+104C>T rs9585366
NM_000282.4(PCCA):c.414+276G>T rs77110421
NM_000282.4(PCCA):c.414+88A>G rs9585365
NM_000282.4(PCCA):c.415-132T>A rs111596243
NM_000282.4(PCCA):c.468+148G>T rs77295050
NM_000282.4(PCCA):c.468+211A>G rs1556800
NM_000282.4(PCCA):c.469-324C>T rs17196604
NM_000282.4(PCCA):c.600+325T>A rs113566641
NM_000282.4(PCCA):c.627A>G (p.Ala209=) rs538229
NM_000282.4(PCCA):c.914+19A>G rs4306370
NM_000282.4(PCCA):c.914+46TTCA[3] rs113891803

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