chr11:27672694:G>C Detail (hg38) (BDNF, BDNF-AS)

Information

Genome

Assembly Position
hg19 chr11:27,694,241-27,694,241 View the variant detail on this assembly version.
hg38 chr11:27,672,694-27,672,694

HGVS

Type Transcript Protein
RefSeq NM_170731.4:c.4-14109C>G
NM_001709.4:c.-21-14109C>G
NM_001143806.1:c.-21-14109C>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 113505 OMIM
HGNC 1033 HGNC
Ensembl ENSG00000176697 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv164301121 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Likely risk allele 2023-12-11 no assertion criteria provided post-traumatic stress disorder inherited Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_001709.5(BDNF):c.[*1785G>T;-21-14109C>G196G>A] AND Post-traumatic stress disorder ClinVar Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs6265 dbSNP
Genome
hg38
Position
chr11:27,672,694-27,672,694
Variant Type
snv
Reference Allele
G
Alternative Allele
C
Genome browser