Variant #0000543673 (NC_000011.9:g.27695665A>G, NM_170735.5:c.-15554T>C (BDNF))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27695665A>G
DNA change (hg38) g.27674118A>G
Published as BDNF(NM_001143810.1):c.167T>C (p.(Val56Ala), p.V56A), BDNF(NM_001143810.2):c.167T>C (p.V56A)
ISCN -
DB-ID BDNF-AS_000001 See all 3 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) 0.00011 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BDNF NM_170735.5 -?/. - c.-15554T>C r.(?) p.(=)
BDNF-AS NR_002832.2 -?/. - n.655-1179A>G r.(?) -


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