Variant #0000548613 (NC_000012.11:g.53345296G>C, NM_199187.1:c.689G>C (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.53345296G>C
DNA change (hg38) g.52951512G>C
Published as KRT18(NM_000224.2):c.689G>C (p.(Ser230Thr))
ISCN -
DB-ID KRT8_000025
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) 0.00354 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT8 NM_002273.3 -?/. - c.-46531C>G r.(?) p.(=)
KRT18 NM_199187.1 -?/. - c.689G>C r.(?) p.(Ser230Thr)


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