Variant #0001068024 (NC_000009.11:g.136501834T>C, NC_000009.11(NM_000787.3):c.339+2T>C (DBH))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.136501834T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID DBH_000003 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs74853476
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00071 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-02 11:48:02 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DBH NM_000787.3 +/. - c.339+2T>C r.(?) p.(?)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.