ClinVar Miner

List of variants reported as risk factor for nervous system cancer

Included ClinVar conditions (64):
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ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_001276270.2(MBD4):c.1544-1G>T rs778697654 0.00005
NM_001276270.2(MBD4):c.1670T>A (p.Leu557Ter) rs200758755 0.00004
NM_000059.4(BRCA2):c.5645C>G (p.Ser1882Ter) rs80358785
NM_000059.4(BRCA2):c.658_659del (p.Val220fs) rs80359604
NM_001276270.2(MBD4):c.1384C>T (p.Arg462Trp) rs1380952147
NM_001276270.2(MBD4):c.1688G>A (p.Trp563Ter) rs939751619
NM_004656.4(BAP1):c.1717del (p.Leu573fs) rs869025212
NM_004656.4(BAP1):c.79del (p.Val27fs) rs397509413
NM_032489.3(ACRBP):c.1040dup (p.Tyr348fs) rs1949067963

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