ClinVar Miner

List of variants in gene KRT12 reported as not provided

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_000223.4(KRT12):c.43C>T (p.Pro15Ser) rs11650915 0.28816
NM_000223.3(KRT12):c.*360A>C rs62065925 0.01366
NM_000223.4(KRT12):c.1276A>G (p.Ile426Val) rs59465138
NM_000223.4(KRT12):c.1277T>G (p.Ile426Ser) rs59350319
NM_000223.4(KRT12):c.1285T>G (p.Tyr429Asp) rs58162394
NM_000223.4(KRT12):c.1286A>G (p.Tyr429Cys) rs59202432
NM_000223.4(KRT12):c.1289G>C (p.Arg430Pro) rs62635290
NM_000223.4(KRT12):c.1298T>G (p.Leu433Arg) rs267607386
NM_000223.4(KRT12):c.385A>G (p.Met129Val) rs267607387
NM_000223.4(KRT12):c.386T>C (p.Met129Thr) rs28936695
NM_000223.4(KRT12):c.389A>C (p.Gln130Pro) rs58864803
NM_000223.4(KRT12):c.399T>G (p.Asn133Lys) rs61167390
NM_000223.4(KRT12):c.403A>G (p.Arg135Gly) rs58410481
NM_000223.4(KRT12):c.404G>C (p.Arg135Thr) rs57218384
NM_000223.4(KRT12):c.404G>T (p.Arg135Ile) rs57218384
NM_000223.4(KRT12):c.405A>C (p.Arg135Ser) rs61282718
NM_000223.4(KRT12):c.409G>C (p.Ala137Pro) rs58038639
NM_000223.4(KRT12):c.419T>G (p.Leu140Arg) rs58918655
NM_000223.4(KRT12):c.427G>C (p.Val143Leu) rs58343600
NM_000223.4(KRT12):c.427G>T (p.Val143Leu) rs58343600
NM_000223.4(KRT12):c.55C>T (p.Arg19Trp) rs200258980

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