ClinVar Miner

List of variants in gene WNT1 reported as pathogenic for not provided

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_005430.4(WNT1):c.506G>A (p.Gly169Asp) rs371672410 0.00009
NM_005430.4(WNT1):c.1005_1027del (p.Thr336fs) rs1190044936
NM_005430.4(WNT1):c.1026del (p.Glu343fs) rs727505392
NM_005430.4(WNT1):c.102G>A (p.Trp34Ter)
NM_005430.4(WNT1):c.1035C>A (p.Cys345Ter)
NM_005430.4(WNT1):c.104+1G>A
NM_005430.4(WNT1):c.287_300del (p.Gln96fs) rs1267271862
NM_005430.4(WNT1):c.364C>T (p.Arg122Ter) rs769853984
NM_005430.4(WNT1):c.3G>A (p.Met1Ile)
NM_005430.4(WNT1):c.479_480del (p.Pro160fs) rs2137624355
NM_005430.4(WNT1):c.499dup (p.Trp167fs) rs892838669
NM_005430.4(WNT1):c.501G>C (p.Trp167Cys) rs1592257435
NM_005430.4(WNT1):c.505G>T (p.Gly169Cys)
NM_005430.4(WNT1):c.506dup (p.Cys170fs) rs779969402
NM_005430.4(WNT1):c.547del (p.Glu183fs)
NM_005430.4(WNT1):c.578del (p.Asp193fs)
NM_005430.4(WNT1):c.681C>A (p.Cys227Ter) rs2137625115
NM_005430.4(WNT1):c.707del (p.Leu236fs)
NM_005430.4(WNT1):c.884C>A (p.Ser295Ter) rs387907356
NM_005430.4(WNT1):c.907G>T (p.Gly303Ter) rs1941012869
NM_005430.4(WNT1):c.953C>A (p.Ser318Ter)
NM_005430.4(WNT1):c.990C>A (p.Cys330Ter)
NM_005430.4(WNT1):c.999_1021del (p.Thr336fs) rs1941014492

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