Variant #0001051803 (NC_000004.11:g.108824504C>T, NM_183075.2:c.-28296C>T (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.108824504C>T
DNA change (hg38) -
Published as SGMS2(NM_001375905.1):c.689C>T (p.(Thr230Met))
ISCN -
DB-ID CYP2U1_000039
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
SGMS2 NM_152621.5 ?/. - c.689C>T r.(?) p.(Thr230Met) -
CYP2U1 NM_183075.2 ?/. - c.-28296C>T r.(?) p.(=) -


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