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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 48

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HGVS	dbSNP	gnomAD frequency
NM_002282.3(KRT83):c.1477C>T (p.His493Tyr)	rs2857671	0.73262
NM_002282.3(KRT83):c.750+15A>G	rs2248619	0.71624
NM_002282.3(KRT83):c.1332T>C (p.Asp444=)	rs2857670	0.71131
NM_002282.3(KRT83):c.*174C>T	rs2852456	0.71024
NM_002282.3(KRT83):c.984C>T (p.Asn328=)	rs2257286	0.41938
NM_002282.3(KRT83):c.1041+6A>G	rs2270267	0.41906
NM_002282.3(KRT83):c.843C>T (p.Ala281=)	rs2857669	0.41821
NM_002282.3(KRT83):c.1056A>G (p.Glu352=)	rs2248473	0.41742
NM_002282.3(KRT83):c.1059T>C (p.Ala353=)	rs2852468	0.41728
NM_002282.3(KRT83):c.*138C>T	rs2857672	0.39671
NM_002282.3(KRT83):c.837C>G (p.Ile279Met)	rs2852464	0.38611
NM_002282.3(KRT83):c.558C>T (p.Asn186=)	rs3741715	0.32296
NM_002282.3(KRT83):c.445C>T (p.Arg149Cys)	rs2857663	0.11683
NM_002282.3(KRT83):c.67T>G (p.Cys23Gly)	rs61485872	0.01374
NM_002282.3(KRT83):c.1084G>A (p.Gly362Ser)	rs140635030	0.01341
NM_002282.3(KRT83):c.1412G>A (p.Gly471Asp)	rs147359482	0.01317
NM_002282.3(KRT83):c.601G>T (p.Glu201Ter)	rs146753414	0.01263
NM_002282.3(KRT83):c.480T>C (p.Phe160=)	rs11834565	0.00832
NM_002282.3(KRT83):c.312G>A (p.Ala104=)	rs111267865	0.00509
NM_002282.3(KRT83):c.1338C>T (p.Cys446=)	rs11836080	0.00309
NM_002282.3(KRT83):c.1042-4C>A	rs200402665	0.00242
NM_002282.3(KRT83):c.1268G>C (p.Cys423Ser)	rs148757217	0.00240
NM_002282.3(KRT83):c.768A>G (p.Gln256=)	rs143202217	0.00170
NM_002282.3(KRT83):c.760A>G (p.Ile254Val)	rs150867374	0.00168
NM_002282.3(KRT83):c.1327G>A (p.Gly443Arg)	rs144061807	0.00091
NM_002282.3(KRT83):c.699C>T (p.Asn233=)	rs186866078	0.00061
NM_002282.3(KRT83):c.1017C>T (p.Ala339=)	rs143467763	0.00041
NM_002282.3(KRT83):c.877C>T (p.Arg293Cys)	rs143037477	0.00035
NM_002282.3(KRT83):c.389G>A (p.Arg130His)	rs139360978	0.00028
NM_002282.3(KRT83):c.*23G>T	rs535186700	0.00027
NM_002282.3(KRT83):c.633C>T (p.Asn211=)	rs140012906	0.00026
NM_002282.3(KRT83):c.1100G>A (p.Ser367Asn)	rs528339841	0.00023
NM_002282.3(KRT83):c.452G>A (p.Cys151Tyr)	rs201680950	0.00019
NM_002282.3(KRT83):c.676C>T (p.Arg226Cys)	rs192947508	0.00015
NM_002282.3(KRT83):c.192C>A (p.Cys64Ter)	rs199997738	0.00014
NM_002282.3(KRT83):c.790G>A (p.Val264Met)	rs201459857	0.00012
NM_002282.3(KRT83):c.1423C>T (p.Pro475Ser)	rs200232339	0.00009
NM_002282.3(KRT83):c.1041+5C>T	rs377435485	0.00006
NM_002282.3(KRT83):c.828G>A (p.Met276Ile)	rs200274404	0.00005
NM_002282.3(KRT83):c.945G>A (p.Arg315=)	rs138807826	0.00004
NM_002282.3(KRT83):c.147C>A (p.Gly49=)	rs542978203	0.00003
NM_002282.3(KRT83):c.497C>G (p.Thr166Ser)	rs200690744	0.00003
NM_002282.3(KRT83):c.910A>T (p.Ser304Cys)	rs770757336	0.00003
NM_002282.3(KRT83):c.593+15G>A	rs756856491	0.00001
NM_002282.3(KRT83):c.*324del	rs11285858
NM_002282.3(KRT83):c.363A>G (p.Arg121=)	rs571144595
NM_002282.3(KRT83):c.520G>C (p.Val174Leu)	rs181439241
NM_002282.3(KRT83):c.666C>T (p.Cys222=)	rs2857667

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