Variant #0001034248 (NC_000004.11:g.108829777G>A, NM_183075.2:c.-23023G>A (CYP2U1))

Chromosome 4
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.108829777G>A
DNA change (hg38) -
Published as SGMS2(NM_001375905.1):c.784G>A (p.(Gly262Arg))
ISCN -
DB-ID CYP2U1_000035
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) 1.0E-5 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 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     
SGMS2 NM_152621.5 ?/. - c.784G>A r.(?) p.(Gly262Arg) -
CYP2U1 NM_183075.2 ?/. - c.-23023G>A r.(?) p.(=) -


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