Variant #0001025963 (NC_000011.9:g.27680005C>T, NM_170735.5:c.107G>A (BDNF))

Chromosome 11
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.27680005C>T
DNA change (hg38) -
Published as BDNF(NM_170735.6):c.107G>A (p.G36D)
ISCN -
DB-ID BDNF_000008 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) 0 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 2025-02-07 18:57:27 +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     
BDNF NM_170735.5 ?/. - c.107G>A r.(?) p.(Gly36Asp)
BDNF-AS NR_002832.2 ?/. - n.592C>T r.(?) -


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