Variant #0001013924 (NC_000004.11:g.108866485T>C, NM_183075.2:c.850T>C (CYP2U1))

Chromosome 4
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.108866485T>C
DNA change (hg38) -
Published as CYP2U1(NM_183075.2):c.850T>C (p.F284L), CYP2U1(NM_183075.3):c.850T>C (p.F284L)
ISCN -
DB-ID CYP2U1_000021 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) 0.00183 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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP2U1 NM_183075.2 -?/. - c.850T>C r.(?) p.(Phe284Leu) -


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