ClinVar Miner

List of variants in gene WWOX reported as likely pathogenic

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Gene type:
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Total variants: 20
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HGVS dbSNP
GRCh37/hg19 16q23.1(chr16:78159696-78320350)x0
GRCh37/hg19 16q23.1(chr16:78198080-78198186)
NC_000016.10:g.(?_78278583)_(78432772_?)del
NC_000016.10:g.(?_78424850)_(78425075_?)del
NM_016373.4(WWOX):c.1043del (p.Phe348fs) rs1064795117
NM_016373.4(WWOX):c.107+2_107+5del rs1555532979
NM_016373.4(WWOX):c.108-2A>T rs1597207802
NM_016373.4(WWOX):c.136C>T (p.His46Tyr) rs1597207871
NM_016373.4(WWOX):c.172G>A (p.Asp58Asn) rs1131691285
NM_016373.4(WWOX):c.183C>A (p.Tyr61Ter) rs759766243
NM_016373.4(WWOX):c.214C>T (p.Gln72Ter) rs201008667
NM_016373.4(WWOX):c.409+1G>C rs1060502727
NM_016373.4(WWOX):c.511G>T (p.Glu171Ter) rs751181600
NM_016373.4(WWOX):c.583G>T (p.Glu195Ter) rs1567542020
NM_016373.4(WWOX):c.605+5G>A rs1039151413
NM_016373.4(WWOX):c.606-1G>A rs730882215
NM_016373.4(WWOX):c.689A>C (p.Gln230Pro)
NM_016373.4(WWOX):c.749C>G (p.Ser250Ter) rs368928190
NM_016373.4(WWOX):c.791+1G>A rs1164465811
NM_016373.4(WWOX):c.918del (p.Glu306fs) rs1057518795

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