Variant #0000259248 (NC_000011.9:g.27679662T>C, NM_170735.5:c.450= (BDNF))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27679662T>C
DNA change (hg38) g.27658115=
Published as BDNF(NM_170735.6):c.450A>G (p.A150=), BDNF-AS(NR_002832.2):n.375-126T>C
ISCN -
DB-ID BDNF_000001
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) 0.99908 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BDNF NM_170735.5 -/. - c.450= r.(=) p.(Ala150=)
BDNF-AS NR_002832.2 -/. - n.375-126T>C r.(?) -


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