Variant #0000805837 (NC_000012.11:g.53298470_53298472del, NM_199187.1:c.-44254_-44252del (KRT18))

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.53298470_53298472del
DNA change (hg38) -
Published as KRT8(NM_001256282.1):c.384_386del (p.(Asn128del))
ISCN -
DB-ID KRT8_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
KRT8 NM_002273.3 ?/. - c.300_302del r.(?) p.(Asn100del)
KRT18 NM_199187.1 ?/. - c.-44254_-44252del r.(?) p.(=)


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