Annotation Detail
Information
- Associated Genes
- BDNF BDNF-AS
- Associated Variants
-
BDNF c.*1785G>T
(
ENST00000438929.5,
ENST00000533131.5,
ENST00000525528.1,
ENST00000395978.7,
ENST00000525950.5,
ENST00000533246.5,
ENST00000418212.5,
ENST00000395983.7,
ENST00000395986.6,
ENST00000439476.6,
ENST00000530861.5,
ENST00000356660.9,
ENST00000314915.6,
ENST00000532997.5,
ENST00000395981.7 )
BDNF p.Val148Met (p.V148M) ( ENST00000532997.5, ENST00000395981.7, ENST00000356660.9, ENST00000314915.6, ENST00000439476.6, ENST00000530861.5, ENST00000395983.7, ENST00000395986.6, ENST00000525950.5, ENST00000533246.5, ENST00000418212.5, ENST00000525528.1, ENST00000533131.5, ENST00000395978.7, ENST00000438929.5 )
BDNF c.225+1366C>G ( ENST00000438929.5, ENST00000395978.7, ENST00000533131.5, ENST00000525950.5, ENST00000533246.5, ENST00000418212.5, ENST00000395986.6, ENST00000395983.7, ENST00000530861.5, ENST00000314915.6, ENST00000356660.9, ENST00000532997.5, ENST00000395981.7 )
BDNF c.*1785G>T ( ENST00000314915.6, ENST00000356660.9, ENST00000395978.7, ENST00000395981.7, ENST00000395983.7, ENST00000395986.6, ENST00000418212.5, ENST00000438929.5, ENST00000439476.6, ENST00000525528.1, ENST00000525950.5, ENST00000530861.5, ENST00000532997.5, ENST00000533131.5, ENST00000533246.5 )
BDNF p.Val148Met (p.V148M) ( ENST00000314915.6, ENST00000356660.9, ENST00000395978.7, ENST00000395981.7, ENST00000395983.7, ENST00000395986.6, ENST00000418212.5, ENST00000438929.5, ENST00000439476.6, ENST00000525528.1, ENST00000525950.5, ENST00000530861.5, ENST00000532997.5, ENST00000533131.5, ENST00000533246.5 )
BDNF c.225+1366C>G ( ENST00000314915.6, ENST00000356660.9, ENST00000395978.7, ENST00000395981.7, ENST00000395983.7, ENST00000395986.6, ENST00000418212.5, ENST00000438929.5, ENST00000525950.5, ENST00000530861.5, ENST00000532997.5, ENST00000533131.5, ENST00000533246.5 ) - Associated Disease
- post-traumatic stress disorder
- Source Database
- ClinVar
- Description
- NM_001709.5(BDNF):c.[*1785G>T;-21-14109C>G196G>A] AND Post-traumatic stress disorder
- ClinVar Allele ID
- 3184387
- ClinVar Allele ID
- 3184388
- ClinVar Allele ID
- 32736
- ClinVar RefSeq Alternation Syntax
- NM_001709.5:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143806.1:c.-21-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_170733.4:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143810.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_170732.4:c.*1784G>T
- ClinVar RefSeq Alternation Syntax
- NM_170734.4:c.241G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143814.2:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143816.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143812.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143809.2:c.67-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143814.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_170731.5:c.4-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_170734.4:c.25-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143807.2:c.-21-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143806.1:c.*1784G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143808.2:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_170734.4:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_170733.4:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NR_033313.1:n.434C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143805.1:c.*1784G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143809.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143806.1:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143808.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143807.2:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143812.2:c.-21-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_170731.5:c.220G>A
- ClinVar RefSeq Alternation Syntax
- NM_170735.6:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143807.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NR_033312.1:n.434C>T
- ClinVar RefSeq Alternation Syntax
- NM_170735.6:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_170732.4:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143805.1:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_170731.5:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143810.2:c.225+1366C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143814.2:c.-128-13768C>G
- ClinVar RefSeq Alternation Syntax
- NR_033315.1:n.434C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143816.2:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NR_033314.1:n.503C>T
- ClinVar RefSeq Alternation Syntax
- NM_001709.5:c.-21-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143813.2:c.-21-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143810.2:c.442G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143813.2:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_170733.4:c.-21-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143811.2:c.-139+1366C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143811.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_170732.4:c.-21-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143813.2:c.*1785G>T
- ClinVar RefSeq Alternation Syntax
- NM_001143811.2:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143809.2:c.283G>A
- ClinVar RefSeq Alternation Syntax
- NM_001709.5:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NM_001143812.2:c.196G>A
- ClinVar RefSeq Alternation Syntax
- NR_002832.2:n.503C>T
- ClinVar RefSeq Alternation Syntax
- NM_001143805.1:c.-21-14109C>G
- ClinVar RefSeq Alternation Syntax
- NM_001143808.2:c.-21-14109C>G
- Clinical Significance Description
- Likely risk allele
- Clinical Significance Last Update
- 2023-12-11
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003881714
- ClinVar Disease
- Post-traumatic stress disorder
- Observed Origin Sample
- inherited
Drugs