ClinVar Miner

List of variants reported as uncertain significance for benign neoplasm of skin by Illumina Laboratory Services, Illumina

Included ClinVar conditions (30):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_153490.3(KRT13):c.*228C>G rs574184263 0.00022
NM_002272.4(KRT4):c.*289G>A rs886049639 0.00010
NM_002272.4(KRT4):c.1417A>T (p.Ser473Cys) rs367751022 0.00008
NM_002272.4(KRT4):c.364C>G (p.Leu122Val) rs758695571 0.00007
NM_002272.4(KRT4):c.405G>A (p.Thr135=) rs762792489 0.00004
NM_153490.3(KRT13):c.759G>C (p.Gln253His) rs766894151 0.00004
NM_002272.4(KRT4):c.317C>G (p.Ala106Gly) rs753431318 0.00003
NM_153490.3(KRT13):c.*175G>A rs1459808765 0.00003
NM_153490.3(KRT13):c.1350C>T (p.Arg450=) rs140142101 0.00003
NM_153490.3(KRT13):c.991C>T (p.Leu331=) rs771435962 0.00003
NM_002272.4(KRT4):c.*496T>G rs753033796 0.00002
NM_002272.4(KRT4):c.193G>A (p.Val65Met) rs754420448 0.00002
NM_153490.3(KRT13):c.1295C>G (p.Ser432Cys) rs1394162514 0.00002
NM_002272.4(KRT4):c.1347-3C>T rs777376453 0.00001
NM_002272.4(KRT4):c.1441G>A (p.Gly481Arg) rs771250577 0.00001
NM_002272.4(KRT4):c.457G>A (p.Asp153Asn) rs780754412 0.00001
NM_002272.4(KRT4):c.677+4C>T rs886049642 0.00001
NM_002272.4(KRT4):c.678-10C>T rs777722293 0.00001
NM_153490.3(KRT13):c.*74A>C rs886052907 0.00001
NM_153490.3(KRT13):c.1220G>A (p.Ser407Asn) rs1265435884 0.00001
NM_153490.3(KRT13):c.337G>A (p.Asp113Asn) rs886052908 0.00001
NM_153490.3(KRT13):c.496-9A>G rs780820686 0.00001
NM_153490.3(KRT13):c.823G>A (p.Ala275Thr) rs767618537 0.00001
NM_002272.4(KRT4):c.*126C>A rs886049640
NM_002272.4(KRT4):c.*405G>A rs886049638
NM_002272.4(KRT4):c.1072C>G (p.Leu358Val) rs1939839883
NM_002272.4(KRT4):c.1467C>A (p.Gly489=) rs1345230715
NM_002272.4(KRT4):c.186C>T (p.Ser62=) rs886049645
NM_002272.4(KRT4):c.25C>G (p.Arg9Gly) rs886049646
NM_002272.4(KRT4):c.353T>G (p.Leu118Trp) rs886049644
NM_002272.4(KRT4):c.463-9T>C rs886049643
NM_002272.4(KRT4):c.54C>G (p.Gly18=) rs748727199
NM_002272.4(KRT4):c.726G>A (p.Val242=) rs886049641
NM_002272.4(KRT4):c.741C>G (p.Asp247Glu) rs369593094
NM_002272.4(KRT4):c.834+2T>G rs937464890
NM_153490.3(KRT13):c.*162T>C rs1904829902
NM_153490.3(KRT13):c.*19C>T rs760565338
NM_153490.3(KRT13):c.*85C>T rs886052906
NM_153490.3(KRT13):c.523C>G (p.Arg175Gly) rs764088068
NM_153490.3(KRT13):c.540T>C (p.Ile180=) rs755205284
NM_153490.3(KRT13):c.853G>A (p.Ala285Thr) rs1904920258

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