ClinVar Miner

List of variants in gene KRT10 reported as not provided by Epithelial Biology; Institute of Medical Biology, Singapore

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Gene type:
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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_000421.5(KRT10):c.376G>A (p.Gly126Ser) rs77919366 0.17640
NM_000421.5(KRT10):c.1264_1265delinsGA (p.Arg422Glu) rs59075499
NM_000421.5(KRT10):c.1281_1282delinsAA (p.Cys427_Gln428delinsTer) rs267607377
NM_000421.5(KRT10):c.1300C>T (p.Gln434Ter) rs60035576
NM_000421.5(KRT10):c.1314_1315insC (p.Lys439fs) rs267607379
NM_000421.5(KRT10):c.1315A>G (p.Lys439Glu) rs61434181
NM_000421.5(KRT10):c.1325T>A (p.Leu442Gln) rs58026994
NM_000421.5(KRT10):c.1333G>A (p.Glu445Lys) rs267607380
NM_000421.5(KRT10):c.1337T>C (p.Ile446Thr) rs62651994
NM_000421.5(KRT10):c.1340A>C (p.Gln447Pro) rs267607378
NM_000421.5(KRT10):c.1346A>G (p.Tyr449Cys) rs267607383
NM_000421.5(KRT10):c.1355T>C (p.Leu452Pro) rs62651995
NM_000421.5(KRT10):c.1358T>C (p.Leu453Pro) rs62652043
NM_000421.5(KRT10):c.1450_1451insC (p.Gly484fs) rs267607382
NM_000421.5(KRT10):c.1546_1551delinsT (p.Gly516fs) rs267607385
NM_000421.5(KRT10):c.1560_1561del (p.Gly521fs) rs267607384
NM_000421.5(KRT10):c.449T>C (p.Met150Thr) rs58901407
NM_000421.5(KRT10):c.449T>G (p.Met150Arg) rs58901407
NM_000421.5(KRT10):c.457C>G (p.Leu153Val) rs61460100
NM_000421.5(KRT10):c.460A>C (p.Asn154His) rs57784225
NM_000421.5(KRT10):c.465_466delinsAA (p.Asp155_Arg156delinsGluSer) rs60712939
NM_000421.5(KRT10):c.466C>A (p.Arg156Ser) rs58852768
NM_000421.5(KRT10):c.466C>G (p.Arg156Gly) rs58852768
NM_000421.5(KRT10):c.466C>T (p.Arg156Cys) rs58852768
NM_000421.5(KRT10):c.467G>A (p.Arg156His) rs58075662
NM_000421.5(KRT10):c.467G>C (p.Arg156Pro) rs58075662
NM_000421.5(KRT10):c.467G>T (p.Arg156Leu) rs58075662
NM_000421.5(KRT10):c.472G>C (p.Ala158Pro) rs59175042
NM_000421.5(KRT10):c.478T>G (p.Tyr160Asp) rs58414354
NM_000421.5(KRT10):c.479A>C (p.Tyr160Ser) rs58735429
NM_000421.5(KRT10):c.481_486del (p.Leu161_Asp162del) rs56809156
NM_000421.5(KRT10):c.482T>C (p.Leu161Ser) rs60118264

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