chr9:84668501:C>G Detail (hg38) (NTRK2)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr9:87,283,416-87,283,416 View the variant detail on this assembly version. |
| hg38 | chr9:84,668,501-84,668,501 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | ||
| Ensemble | ENST00000686259.1:c.-866C>G | |
| ENST00000686496.1:c.-1321C>G |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.042 | major depressive disorder | We genotyped the BDNF gene Val66Met (rs6265) polymorphism and four single-nucleo... | BeFree | 20014955 | Detail |
| 0.002 | major depressive disorder | We genotyped the BDNF gene Val66Met (rs6265) polymorphism and four single-nucleo... | BeFree | 20014955 | Detail |
| 0.002 | Unipolar Depression | We genotyped the BDNF gene Val66Met (rs6265) polymorphism and four single-nucleo... | BeFree | 20014955 | Detail |
| 0.022 | Unipolar Depression | We genotyped the BDNF gene Val66Met (rs6265) polymorphism and four single-nucleo... | BeFree | 20014955 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| We genotyped the BDNF gene Val66Met (rs6265) polymorphism and four single-nucleotide polymorphisms (... | DisGeNET | Detail |
| We genotyped the BDNF gene Val66Met (rs6265) polymorphism and four single-nucleotide polymorphisms (... | DisGeNET | Detail |
| We genotyped the BDNF gene Val66Met (rs6265) polymorphism and four single-nucleotide polymorphisms (... | DisGeNET | Detail |
| We genotyped the BDNF gene Val66Met (rs6265) polymorphism and four single-nucleotide polymorphisms (... | DisGeNET | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs1187323 dbSNP
- Genome
- hg38
- Position
- chr9:84,668,501-84,668,501
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- G
Genome browser