Variant #0000281939 (NC_000012.11:g.52685096C>G, NM_002284.3:c.-10605C>G (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.52685096C>G
DNA change (hg38) g.52291312C>G
Published as KRT81(NM_002281.4):c.154G>C (p.G52R)
ISCN -
DB-ID KRT81_000013
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) 0.31669 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-12-07 15:54:23 +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.154G>C r.(?) p.(Gly52Arg)
KRT86 NM_002284.3 -/. - c.-10605C>G r.(?) p.(=)


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