ClinVar Miner

List of variants in gene WWOX reported as pathogenic

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Gene type:
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Total variants: 27
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HGVS dbSNP
GRCh37/hg19 16q23.1(chr16:78143268-78154701)
GRCh37/hg19 16q23.1(chr16:78180603-78208482)x0
GRCh37/hg19 16q23.1(chr16:78409180-78431277)
GRCh37/hg19 16q23.1(chr16:78458774-78463512)
NC_000016.10:g.(?_78164163)_(78164309_?)del
NC_000016.10:g.(?_78318746)_(78386940_?)dup
NC_000016.10:g.(?_78386840)_(78386968_?)del
NC_000016.10:g.(?_78432468)_(78432772_?)del
NM_016373.2(WWOX):c.131G>A (p.Trp44Ter) rs1057517846
NM_016373.2(WWOX):c.132G>A (p.Trp44Ter) rs1555535072
NM_016373.2(WWOX):c.255C>G (p.Tyr85Ter) rs990150249
NM_016373.2(WWOX):c.410-1G>A rs886039653
NM_016373.2(WWOX):c.517-?_605+?del
NM_016373.3(WWOX):c.-366-?_516+?del
NM_016373.3(WWOX):c.1005G>A (p.Trp335Ter) rs730880290
NM_016373.3(WWOX):c.139C>A (p.Pro47Thr) rs587777128
NM_016373.3(WWOX):c.140C>G (p.Pro47Arg) rs730880292
NM_016373.3(WWOX):c.160C>T (p.Arg54Ter) rs587777248
NM_016373.3(WWOX):c.46_49del (p.Asp16Serfs) rs730880291
NM_016373.3(WWOX):c.517-?_605+?del
NM_016373.3(WWOX):c.749C>G (p.Ser250Ter) rs368928190
NM_016373.3(WWOX):c.754C>G (p.Pro252Ala) rs75559202
NM_016373.3(WWOX):c.779C>G (p.Ser260Ter) rs878855021
NM_016373.3(WWOX):c.790C>T (p.Arg264Ter) rs756762196
NM_016373.3(WWOX):c.872T>C (p.Leu291Pro) rs119487098
NM_016373.3(WWOX):c.990C>G (p.Asn330Lys) rs117209694
NM_016373.4(WWOX):c.583G>T (p.Glu195Ter)

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