Variant #0000959691 (NC_000015.9:g.74631641G>A, NM_000781.2:c.1173C>T (CYP11A1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74631641G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CYP11A1_000015
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs751829411
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-02-01 10:08:01 +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     
CYP11A1 NM_000781.2 +?/. - c.1173C>T r.(?) p.(Ser391=) -


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