Variant #0000270672 (NC_000010.10:g.94822756C>T, NC_000010.10(NM_183374.2):c.705+4C>T (CYP26C1))

Chromosome 10
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.94822756C>T
DNA change (hg38) g.93062999C>T
Published as CYP26C1(NM_183374.3):c.705+4C>T
ISCN -
DB-ID CYP26C1_000007
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) 0.0161 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     

Haplotype     
EXOC6 NM_019053.4 -/. - c.*4644C>T r.(=) p.(=) -
CYP26C1 NM_183374.2 -/. - c.705+4C>T r.spl? p.? -


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