Variant #0000548610 (NC_000012.11:g.53343273C>T, NM_199187.1:c.316C>T (KRT18))

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.53343273C>T
DNA change (hg38) g.52949489C>T
Published as KRT18(NM_000224.3):c.316C>T (p.R106W), KRT8(NM_001256293.2):c.-47+226G>A
ISCN -
DB-ID KRT8_000022
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT8 NM_002273.3 -/. - c.-44508G>A r.(?) p.(=)
KRT18 NM_199187.1 -/. - c.316C>T r.(?) p.(Arg106Trp)


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