ClinVar Miner

List of variants in gene KRT24 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_019016.3(KRT24):c.1214C>T (p.Thr405Met) rs149979571 0.00029
NM_019016.3(KRT24):c.1447T>C (p.Ser483Pro) rs202143442 0.00017
NM_019016.3(KRT24):c.319G>A (p.Gly107Arg) rs137997447 0.00013
NM_019016.3(KRT24):c.448C>T (p.Arg150Cys) rs146935622 0.00007
NM_019016.3(KRT24):c.556G>A (p.Gly186Ser) rs201821647 0.00007
NM_019016.3(KRT24):c.185G>A (p.Gly62Asp) rs772286667 0.00006
NM_019016.3(KRT24):c.1234G>A (p.Glu412Lys) rs752427510 0.00004
NM_019016.3(KRT24):c.727A>G (p.Ser243Gly) rs749993304 0.00004
NM_019016.3(KRT24):c.817A>T (p.Thr273Ser) rs750035114 0.00004
NM_019016.3(KRT24):c.1454G>A (p.Ser485Asn) rs747547032 0.00003
NM_019016.3(KRT24):c.250G>A (p.Gly84Arg) rs778370523 0.00003
NM_019016.3(KRT24):c.721C>T (p.Arg241Trp) rs753543063 0.00002
NM_019016.3(KRT24):c.1003C>T (p.Arg335Trp) rs370798217 0.00001
NM_019016.3(KRT24):c.1028T>C (p.Leu343Pro) rs2037657985 0.00001
NM_019016.3(KRT24):c.1057G>A (p.Ala353Thr) rs762507336 0.00001
NM_019016.3(KRT24):c.1192G>C (p.Ala398Pro) rs762033241 0.00001
NM_019016.3(KRT24):c.38G>A (p.Gly13Glu) rs373675915 0.00001
NM_019016.3(KRT24):c.622G>A (p.Ala208Thr) rs755078486 0.00001
NM_019016.3(KRT24):c.664A>G (p.Asn222Asp) rs1597777500 0.00001
NM_019016.3(KRT24):c.853G>A (p.Glu285Lys) rs769419981 0.00001
NM_019016.3(KRT24):c.1112T>A (p.Leu371Gln)
NM_019016.3(KRT24):c.1123C>A (p.Leu375Ile)
NM_019016.3(KRT24):c.1189G>A (p.Val397Met)
NM_019016.3(KRT24):c.1272G>C (p.Gln424His)
NM_019016.3(KRT24):c.1358G>A (p.Gly453Glu) rs2508658459
NM_019016.3(KRT24):c.1481G>C (p.Ser494Thr) rs2508656585
NM_019016.3(KRT24):c.1490G>A (p.Arg497Lys)
NM_019016.3(KRT24):c.160G>T (p.Gly54Trp)
NM_019016.3(KRT24):c.17G>A (p.Arg6His)
NM_019016.3(KRT24):c.180T>G (p.Phe60Leu)
NM_019016.3(KRT24):c.200G>T (p.Gly67Val)
NM_019016.3(KRT24):c.233G>A (p.Gly78Glu)
NM_019016.3(KRT24):c.295T>C (p.Phe99Leu)
NM_019016.3(KRT24):c.370G>A (p.Gly124Ser) rs762874562
NM_019016.3(KRT24):c.416G>T (p.Gly139Val) rs1352712252
NM_019016.3(KRT24):c.461A>G (p.Tyr154Cys) rs2508666333
NM_019016.3(KRT24):c.527A>G (p.Tyr176Cys) rs919667400
NM_019016.3(KRT24):c.563C>T (p.Ser188Leu)
NM_019016.3(KRT24):c.626C>T (p.Ala209Val)
NM_019016.3(KRT24):c.652T>G (p.Leu218Val)
NM_019016.3(KRT24):c.684T>A (p.Asp228Glu) rs2508664218
NM_019016.3(KRT24):c.730G>A (p.Val244Met)
NM_019016.3(KRT24):c.820G>A (p.Glu274Lys)
NM_019016.3(KRT24):c.829G>C (p.Ala277Pro) rs374848466
NM_019016.3(KRT24):c.870G>T (p.Met290Ile) rs776464675
NM_019016.3(KRT24):c.913G>A (p.Ala305Thr)

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