ClinVar Miner

List of variants in gene KRT9 reported as uncertain significance for diffuse palmoplantar keratoderma

Included ClinVar conditions (59):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_000226.4(KRT9):c.1560C>T (p.Tyr520=) rs116616468 0.00178
NM_000226.4(KRT9):c.1125C>T (p.His375=) rs114867228 0.00143
NM_000226.4(KRT9):c.1120C>T (p.Arg374Trp) rs116216460 0.00134
NM_000226.4(KRT9):c.*181G>A rs180874109 0.00103
NM_000226.4(KRT9):c.1290C>T (p.Ile430=) rs145501803 0.00093
NM_000226.4(KRT9):c.*318C>T rs573602616 0.00066
NM_000226.4(KRT9):c.-31G>A rs376504688 0.00043
NM_000226.4(KRT9):c.1216T>C (p.Cys406Arg) rs77688767 0.00043
NM_000226.4(KRT9):c.1096A>G (p.Ser366Gly) rs114395985 0.00038
NM_000226.4(KRT9):c.*40+2del rs777438204 0.00037
NM_000226.4(KRT9):c.*309del rs886052909 0.00036
NM_000226.4(KRT9):c.697C>T (p.Arg233Cys) rs144301874 0.00019
NM_000226.4(KRT9):c.*263T>C rs954998850 0.00012
NM_000226.4(KRT9):c.1519G>C (p.Gly507Arg) rs144649847 0.00010
NM_000226.4(KRT9):c.1520G>T (p.Gly507Val) rs149321431 0.00010
NM_000226.4(KRT9):c.286G>A (p.Gly96Ser) rs145530082 0.00010
NM_000226.4(KRT9):c.1594G>A (p.Gly532Ser) rs372549420 0.00009
NM_000226.4(KRT9):c.-23A>G rs753666153 0.00008
NM_000226.4(KRT9):c.1021A>G (p.Ile341Val) rs201833191 0.00008
NM_000226.4(KRT9):c.250A>G (p.Ser84Gly) rs563000405 0.00008
NM_000226.4(KRT9):c.1336C>T (p.Arg446Trp) rs201551901 0.00006
NM_000226.4(KRT9):c.*123T>C rs1444464733 0.00004
NM_000226.4(KRT9):c.1069T>C (p.Ser357Pro) rs146440373 0.00004
NM_000226.4(KRT9):c.1126G>A (p.Gly376Ser) rs200211641 0.00004
NM_000226.4(KRT9):c.1797C>T (p.Ser599=) rs754967566 0.00004
NM_000226.4(KRT9):c.1839C>T (p.Tyr613=) rs142173628 0.00004
NM_000226.4(KRT9):c.291T>C (p.Phe97=) rs376830738 0.00004
NM_000226.4(KRT9):c.-50C>T rs768450433 0.00003
NM_000226.4(KRT9):c.347G>A (p.Gly116Asp) rs746202552 0.00003
NM_000226.4(KRT9):c.121G>A (p.Gly41Ser) rs201530335 0.00002
NM_000226.4(KRT9):c.1394T>G (p.Phe465Cys) rs753893753 0.00002
NM_000226.4(KRT9):c.1549G>A (p.Gly517Arg) rs201495509 0.00002
NM_000226.4(KRT9):c.*103C>G rs886052911 0.00001
NM_000226.4(KRT9):c.*225T>C rs1039328870 0.00001
NM_000226.4(KRT9):c.*230T>C rs886052910 0.00001
NM_000226.4(KRT9):c.*275A>C rs1906858213 0.00001
NM_000226.4(KRT9):c.1119C>T (p.Leu373=) rs537282263 0.00001
NM_000226.4(KRT9):c.1275C>T (p.Asp425=) rs781603266 0.00001
NM_000226.4(KRT9):c.1457G>A (p.Gly486Glu) rs749465914 0.00001
NM_000226.4(KRT9):c.212A>G (p.Tyr71Cys) rs1350886851 0.00001
NM_000226.4(KRT9):c.*41-8C>T rs765440137
NM_000226.4(KRT9):c.*93C>T rs1906863910
NM_000226.4(KRT9):c.1011C>T (p.Asn337=) rs143100726
NM_000226.4(KRT9):c.1045-9G>T rs144984735
NM_000226.4(KRT9):c.1049C>T (p.Thr350Ile) rs1240669066
NM_000226.4(KRT9):c.1127G>A (p.Gly376Asp) rs777254346
NM_000226.4(KRT9):c.1282C>T (p.Gln428Ter)
NM_000226.4(KRT9):c.1315C>T (p.Leu439Phe) rs761629042
NM_000226.4(KRT9):c.1363C>T (p.His455Tyr) rs572344925
NM_000226.4(KRT9):c.1405G>A (p.Gly469Arg) rs201817471
NM_000226.4(KRT9):c.1795A>C (p.Ser599Arg)
NM_000226.4(KRT9):c.1869C>T (p.Ser623=) rs749243428
NM_000226.4(KRT9):c.380A>G (p.Tyr127Cys) rs1907085178
NM_000226.4(KRT9):c.470T>C (p.Met157Thr) rs59510579
NM_000226.4(KRT9):c.532AAC[1] (p.Asn179del) rs1907073179
NM_000226.4(KRT9):c.578G>A (p.Gly193Glu) rs142413684
NM_000226.4(KRT9):c.644T>C (p.Ile215Thr) rs886052912

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