ClinVar Miner

List of variants in gene KRT14 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000526.5(KRT14):c.193C>T (p.Leu65=) rs3826551 0.58145
NM_000526.5(KRT14):c.189C>T (p.Cys63=) rs11551758 0.56357
NM_000526.5(KRT14):c.6C>T (p.Thr2=) rs11551759 0.56334
NM_000526.5(KRT14):c.369T>C (p.Asn123=) rs3826549 0.56333
NM_000526.5(KRT14):c.280G>A (p.Ala94Thr) rs3826550 0.40897
NM_000526.5(KRT14):c.231C>T (p.Ser77=) rs6503639 0.25809
NM_000526.5(KRT14):c.1322-13A>G rs2001185 0.17177
NM_000526.5(KRT14):c.1237G>A (p.Ala413Thr) rs59780231 0.01556
NM_000526.5(KRT14):c.202G>A (p.Gly68Ser) rs142137272 0.00225
NM_000526.5(KRT14):c.54C>T (p.Cys18=) rs60831116 0.00058
NM_000526.5(KRT14):c.1203G>A (p.Leu401=) rs139804375 0.00054
NM_000526.5(KRT14):c.739G>A (p.Ala247Thr) rs574163361 0.00004
NM_000526.5(KRT14):c.-1C>T
NM_000526.5(KRT14):c.182G>A (p.Gly61Glu)
NM_000526.5(KRT14):c.220AGC[4] (p.Ser78_Ser79del) rs747557834
NM_000526.5(KRT14):c.373C>T (p.Arg125Cys) rs60399023
NM_000526.5(KRT14):c.374G>A (p.Arg125His) rs58330629
NM_000526.5(KRT14):c.537C>A (p.Ala179=)
NM_000526.5(KRT14):c.856G>C (p.Glu286Gln)
NM_000526.5(KRT14):c.996G>A (p.Ser332=)

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