Variant #0000548533 (NC_000012.11:g.52696929C>A, NM_002284.3:c.415C>A (KRT86))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52696929C>A
DNA change (hg38) g.52303145C>A
Published as KRT86(NM_001320198.1):c.415C>A (p.Q139K)
ISCN -
DB-ID KRT86_000012
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01121 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT81 NM_002281.3 -/. - c.-11680G>T r.(?) p.(=)
KRT86 NM_002284.3 -/. - c.415C>A r.(?) p.(Gln139Lys)


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