Variant #0001038101 (NC_000010.10:g.94824277_94824283dup, NM_183374.2:c.845_851dup (CYP26C1))

Chromosome 10
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.94824277_94824283dup
DNA change (hg38) -
Published as CYP26C1(NM_183374.3):c.845_851dup (p.(Gln284HisfsTer129)), CYP26C1(NM_183374.3):c.845_851dupCCATGCA (p.Q284Hfs*129)
ISCN -
DB-ID CYP26C1_000009 See all 2 reported entries
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 2025-05-05 21:14:00 +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     

Haplotype     
CYP26C1 NM_183374.2 ?/. - c.845_851dup r.(?) p.(Gln284HisfsTer129) -


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