Variant #0000608968 (NC_000004.11:g.108853216G>T, NM_183075.2:c.417G>T (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.108853216G>T
DNA change (hg38) g.107932060G>T
Published as CYP2U1(NM_183075.3):c.417G>T (p.A139=)
ISCN -
DB-ID CYP2U1_000018
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 14:54:23 +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     
SGMS2 NM_152621.5 -?/. - c.*21507G>T r.(=) p.(=) -
CYP2U1 NM_183075.2 -?/. - c.417G>T r.(?) p.(Ala139=) -


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