ClinVar Miner

List of variants in gene KRT6A reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_005554.4(KRT6A):c.1303C>T (p.Gln435Ter) rs267607467
NM_005554.4(KRT6A):c.1381G>A (p.Glu461Lys) rs267607468
NM_005554.4(KRT6A):c.1381G>C (p.Glu461Gln) rs267607468
NM_005554.4(KRT6A):c.1385T>A (p.Ile462Asn) rs57629991
NM_005554.4(KRT6A):c.1385T>G (p.Ile462Ser) rs57629991
NM_005554.4(KRT6A):c.1387G>C (p.Ala463Pro) rs267607462
NM_005554.4(KRT6A):c.1390A>C (p.Thr464Pro) rs61293647
NM_005554.4(KRT6A):c.1393T>C (p.Tyr465His) rs267607463
NM_005554.4(KRT6A):c.1394A>G (p.Tyr465Cys) rs267607469
NM_005554.4(KRT6A):c.1403T>A (p.Leu468Gln) rs59018888
NM_005554.4(KRT6A):c.1403T>C (p.Leu468Pro) rs59018888
NM_005554.4(KRT6A):c.1406T>C (p.Leu469Pro) rs57052654
NM_005554.4(KRT6A):c.1406T>G (p.Leu469Arg) rs57052654
NM_005554.4(KRT6A):c.1414G>A (p.Glu472Lys) rs60554162
NM_005554.4(KRT6A):c.1416G>C (p.Glu472Asp) rs267607470
NM_005554.4(KRT6A):c.1511dup (p.Ser505fs) rs267607471
NM_005554.4(KRT6A):c.487G>A (p.Glu163Lys) rs267607464
NM_005554.4(KRT6A):c.491G>C (p.Arg164Pro) rs62635293
NM_005554.4(KRT6A):c.497A>C (p.Gln166Pro) rs267607460
NM_005554.4(KRT6A):c.500T>A (p.Ile167Asn) rs57126929
NM_005554.4(KRT6A):c.500T>G (p.Ile167Ser) rs57126929
NM_005554.4(KRT6A):c.508C>T (p.Leu170Phe) rs57448541
NM_005554.4(KRT6A):c.510CAA[2] (p.Asn172del) rs606231214
NM_005554.4(KRT6A):c.511A>G (p.Asn171Asp) rs62635294
NM_005554.4(KRT6A):c.511A>T (p.Asn171Tyr) rs62635294
NM_005554.4(KRT6A):c.512A>C (p.Asn171Thr) rs58556099
NM_005554.4(KRT6A):c.512A>G (p.Asn171Ser) rs58556099
NM_005554.4(KRT6A):c.513C>A (p.Asn171Lys) rs59685571
NM_005554.4(KRT6A):c.520T>G (p.Phe174Val) rs28933087
NM_005554.4(KRT6A):c.521T>C (p.Phe174Ser) rs61145796
NM_005554.4(KRT6A):c.521T>G (p.Phe174Cys) rs61145796
NM_005554.4(KRT6A):c.526T>C (p.Ser176Pro) rs59642296
NM_005554.4(KRT6A):c.533T>A (p.Ile178Asn) rs267607461
NM_005554.4(KRT6A):c.541-1G>C rs267607465
NM_005554.4(KRT6A):c.541-1G>T rs267607465
NM_005554.4(KRT6A):c.541-2A>C rs267607466
NM_005554.4(KRT6A):c.541-2A>G rs267607466

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