Variant #0000980366 (NC_000012.11:g.53344108C>G, NC_000012.11(NM_199187.1):c.418-4C>G (KRT18))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53344108C>G
DNA change (hg38) -
Published as KRT18(NM_000224.3):c.418-4C>G
ISCN -
DB-ID KRT8_000031
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) 0.00117 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
KRT8 NM_002273.3 -?/. - c.-45343G>C r.(?) p.(=)
KRT18 NM_199187.1 -?/. - c.418-4C>G r.spl? p.?


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