ClinVar Miner

List of variants in gene KRT9 reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_000226.4(KRT9):c.1216T>C (p.Cys406Arg) rs77688767 0.00043
NM_000226.4(KRT9):c.488G>A (p.Arg163Gln) rs57758262 0.00001
NM_000226.4(KRT9):c.1360T>C (p.Tyr454His) rs267607420
NM_000226.4(KRT9):c.1363_1365dup (p.His455dup) rs57909628
NM_000226.4(KRT9):c.1372C>T (p.Leu458Phe) rs58120120
NM_000226.4(KRT9):c.216C>T (p.Ser72=) rs57483266
NM_000226.4(KRT9):c.426A>C (p.Gly142=) rs58061921
NM_000226.4(KRT9):c.429A>C (p.Gly143=) rs8075921
NM_000226.4(KRT9):c.469A>G (p.Met157Val) rs58597584
NM_000226.4(KRT9):c.470T>A (p.Met157Lys) rs59510579
NM_000226.4(KRT9):c.470T>C (p.Met157Thr) rs59510579
NM_000226.4(KRT9):c.470T>G (p.Met157Arg) rs59510579
NM_000226.4(KRT9):c.478C>G (p.Leu160Val) rs28940896
NM_000226.4(KRT9):c.478C>T (p.Leu160Phe) rs28940896
NM_000226.4(KRT9):c.481A>C (p.Asn161His) rs59296273
NM_000226.4(KRT9):c.481A>T (p.Asn161Tyr) rs59296273
NM_000226.4(KRT9):c.482A>G (p.Asn161Ser) rs56707768
NM_000226.4(KRT9):c.482A>T (p.Asn161Ile) rs56707768
NM_000226.4(KRT9):c.483T>A (p.Asn161Lys) rs57536312
NM_000226.4(KRT9):c.484T>C (p.Ser162Pro) rs267607419
NM_000226.4(KRT9):c.487C>T (p.Arg163Trp) rs59616921
NM_000226.4(KRT9):c.488G>C (p.Arg163Pro) rs57758262
NM_000226.4(KRT9):c.500delinsGGCT (p.Tyr167delinsTrpLeu) rs59317143
NM_000226.4(KRT9):c.503T>C (p.Leu168Ser) rs61157095
NM_000226.4(KRT9):c.508A>T (p.Lys170Ter) rs58149344
NM_000226.4(KRT9):c.511G>A (p.Val171Met) rs57019720
NM_000226.4(KRT9):c.515A>C (p.Gln172Pro) rs59878153

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