ClinVar Miner

List of variants in gene KRT5 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000424.4(KRT5):c.30G>A (p.Arg10=) rs61747182 0.00780
NM_000424.4(KRT5):c.1071C>T (p.Ala357=) rs149467228 0.00503
NM_000424.4(KRT5):c.1636C>A (p.Leu546Ile) rs114734812 0.00394
NM_000424.4(KRT5):c.381C>T (p.Phe127=) rs150390099 0.00069
NM_000424.4(KRT5):c.39C>T (p.Gly13=) rs116931869 0.00042
NM_000424.4(KRT5):c.216G>A (p.Lys72=) rs141631999 0.00021
NM_000424.4(KRT5):c.1440-6T>C rs374119094 0.00020
NM_000424.4(KRT5):c.1675C>T (p.Arg559Ter) rs754242209 0.00009
NM_000424.4(KRT5):c.280G>A (p.Gly94Ser) rs138806570 0.00009
NM_000424.4(KRT5):c.1561G>A (p.Gly521Ser) rs375140289 0.00007
NM_000424.4(KRT5):c.324C>T (p.Gly108=) rs759191256 0.00007
NM_000424.4(KRT5):c.102C>T (p.Ser34=) rs377261145 0.00005
NM_000424.4(KRT5):c.1616G>A (p.Gly539Asp) rs753029185 0.00003
NM_000424.4(KRT5):c.114C>T (p.Ser38=)
NM_000424.4(KRT5):c.136T>A (p.Phe46Ile)
NM_000424.4(KRT5):c.1440-10C>G
NM_000424.4(KRT5):c.1550_1573del (p.509GGGL[2])
NM_000424.4(KRT5):c.1551C>T (p.Gly517=)
NM_000424.4(KRT5):c.1602C>T (p.Ser534=) rs745858077
NM_000424.4(KRT5):c.1615G>A (p.Gly539Ser)
NM_000424.4(KRT5):c.1677A>T (p.Arg559=) rs1469765298
NM_000424.4(KRT5):c.465G>A (p.Leu155=) rs1445452986
NM_000424.4(KRT5):c.926C>T (p.Ala309Val) rs552561992

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