Annotation Detail
Information
- Associated Genes
- BDNF
- Associated Variants
-
BDNF c.-59+783C>T
(
ENST00000395978.7,
ENST00000438929.5,
ENST00000395983.7,
ENST00000418212.5,
ENST00000533246.5,
ENST00000525950.5,
ENST00000530861.5,
ENST00000395981.7,
ENST00000532997.5,
ENST00000314915.6,
ENST00000356660.9 )
BDNF c.-59+783C>T ( ENST00000314915.6, ENST00000356660.9, ENST00000395978.7, ENST00000395981.7, ENST00000395983.7, ENST00000418212.5, ENST00000438929.5, ENST00000525950.5, ENST00000530861.5, ENST00000532997.5, ENST00000533246.5 ) - Associated Disease
- Variant of unknown significance
- Source Database
- ClinVar
- Description
- NM_001709.5(BDNF):c.-46C>T AND Variant of unknown significance
- ClinVar Allele ID
- 32737
- ClinVar RefSeq Alternation Syntax
- NM_001143809.2:c.66+783C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143814.2:c.-153C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143812.2:c.-22+488C>T
- ClinVar RefSeq Alternation Syntax
- NM_170731.5:c.3+21224C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143805.1:c.-22+20456C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143808.2:c.-22+793C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143806.1:c.-22+20241C>T
- ClinVar RefSeq Alternation Syntax
- NM_170733.4:c.-22+1109C>T
- ClinVar RefSeq Alternation Syntax
- NM_001709.5:c.-46C>T
- ClinVar RefSeq Alternation Syntax
- NM_170732.4:c.-22+20158C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143807.2:c.-22+19323C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143810.2:c.-59+783C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143813.2:c.-28C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143811.2:c.-422+783C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2004-06-15
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000019273
- ClinVar Disease
- Variant of unknown significance
- Observed Origin Sample
- germline
- Pubmed
- 15115760
Drugs