Variant #0000805828 (NC_000012.11:g.52757038G>A, NM_002283.3:c.943C>T (KRT85))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.52757038G>A
DNA change (hg38) -
Published as KRT85(NM_002283.3):c.943C>T (p.R315C), KRT85(NM_002283.4):c.943C>T (p.R315C)
ISCN -
DB-ID KRT85_000003 See all 2 reported entries
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) 2.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT85 NM_002283.3 ?/. - c.943C>T r.(?) p.(Arg315Cys)


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