Variant #0000978495 (NC_000009.11:g.136521738G>A, NM_000787.3:c.1528G>A (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.136521738G>A
DNA change (hg38) -
Published as DBH(NM_000787.3):c.1528G>A (p.G510S), DBH(NM_000787.4):c.1528G>A (p.G510S)
ISCN -
DB-ID DBH_000015 See all 2 reported entries
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) 7.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DBH NM_000787.3 ?/. - c.1528G>A r.(?) p.(Gly510Ser)


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