Variant #0000852872 (NC_000011.9:g.27695732_27695733del, NM_170735.5:c.-15622_-15621del (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.27695732_27695733del
DNA change (hg38) -
Published as BDNF(NM_001143810.1):c.99_100delAT (p.C34Ffs*12), BDNF(NM_001143810.2):c.99_100delAT (p.C34Ffs*12)
ISCN -
DB-ID BDNF-AS_000002 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) 0.00069 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 2022-05-09 15:40:45 +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.-15622_-15621del r.(?) p.(=)
BDNF-AS NR_002832.2 -?/. - n.655-1112_655-1111del r.(?) -


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