Variant #0000723397 (NC_000011.9:g.27695785A>G, NM_170735.5:c.-15674T>C (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.27695785A>G
DNA change (hg38) -
Published as BDNF(NM_001143810.1):c.47T>C (p.L16P), BDNF(NM_001143810.2):c.47T>C (p.L16P)
ISCN -
DB-ID BDNF-AS_000003 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) 0.00258 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.-15674T>C r.(?) p.(=)
BDNF-AS NR_002832.2 -/. - n.655-1059A>G r.(?) -


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