Variant #0000611956 (NC_000009.11:g.136523528_136523529del, NM_000787.3:c.1813_1814del (DBH))

Chromosome 9
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.136523528_136523529del
DNA change (hg38) g.133658406_133658407del
Published as DBH(NM_000787.3):c.1813_1814delGC (p.A605Wfs*59)
ISCN -
DB-ID DBH_000017
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-26 11:41:05 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DBH NM_000787.3 ?/. - c.1813_1814del r.(?) p.(Ala605TrpfsTer59)


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