ClinVar Miner

List of variants in gene KRT83 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_002282.3(KRT83):c.*107T>G rs771547026 0.00035
NM_002282.3(KRT83):c.-58C>A rs573598308 0.00031
NM_002282.3(KRT83):c.*268A>C rs777492822 0.00009
NM_002282.3(KRT83):c.514G>A (p.Glu172Lys) rs140443749 0.00006
NM_002282.3(KRT83):c.*44C>T rs186532103 0.00004
NM_002282.3(KRT83):c.1356G>A (p.Pro452=) rs764238442 0.00004
NM_002282.3(KRT83):c.815G>A (p.Arg272Gln) rs369510264 0.00004
NM_002282.3(KRT83):c.502C>T (p.Arg168Trp) rs778964859 0.00003
NM_002282.3(KRT83):c.1014A>G (p.Thr338=) rs202206430 0.00001
NM_002282.3(KRT83):c.1425C>T (p.Pro475=) rs757638030 0.00001
NM_002282.3(KRT83):c.*102T>G rs955581900
NM_002282.3(KRT83):c.*135C>T rs956056629
NM_002282.3(KRT83):c.*225C>T rs886049620
NM_002282.3(KRT83):c.*60C>A rs1938655369
NM_002282.3(KRT83):c.1398G>A (p.Leu466=) rs748151673
NM_002282.3(KRT83):c.173G>C (p.Gly58Ala) rs776629118
NM_002282.3(KRT83):c.183C>T (p.Ala61=) rs755364196
NM_002282.3(KRT83):c.184G>A (p.Gly62Ser) rs749653752
NM_002282.3(KRT83):c.260C>T (p.Ser87Leu) rs538643123
NM_002282.3(KRT83):c.485G>T (p.Gly162Val) rs140783754
NM_002282.3(KRT83):c.83G>T (p.Ser28Ile) rs886049622
NM_002282.3(KRT83):c.891G>C (p.Glu297Asp) rs886049621

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