chr7:82450035:A>C Detail (hg19) (PCLO)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr7:82,450,035-82,450,035 |
hg38 | chr7:82,820,719-82,820,719 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_033026.5:c.14791+1776T>G | |
NM_014510.2:c.*1759T>G | ||
Ensemble | ENST00000333891.14:c.14791+1776T>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.882 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.130 | major depressive disorder | NA | GAD | Detail | |
0.130 | major depressive disorder | [These results provide genetic basis for gender differences in MDD and will serv... | GAD | 21621269 | Detail |
0.130 | major depressive disorder | Genome-wide association analysis of gender differences in major depressive disor... | GWASCAT | 21621269 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NA | DisGeNET | Detail |
[These results provide genetic basis for gender differences in MDD and will serve as a resource for ... | DisGeNET | Detail |
Genome-wide association analysis of gender differences in major depressive disorder in the Netherlan... | 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
- rs2715148 dbSNP
- Genome
- hg19
- Position
- chr7:82,450,035-82,450,035
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- C
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs2715148
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.8817
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 14775
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16758
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