chr17:61560763:T>C Detail (hg19) (ACE)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr17:61,560,763-61,560,763 |
| hg38 | chr17:63,483,402-63,483,402 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000789.3:c.1488-58T>C | |
| Ensemble | ENST00000428043.5:c.1488-58T>C | |
| ENST00000290866.10:c.1488-58T>C |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.662 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:[No Data.] |
Prediction
ClinVar
| Clinical Significance |
|
| Review star | ![]() |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
|
2018-11-10 | criteria provided, single submitter | not provided |
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.153 | Kidney Diseases | ACE ID/DD genotypes in combination with ACE rs4311, rs4343, and AGT rs699 mutant... | BeFree | 19108684 | Detail |
| 0.003 | Panic Attacks | Here we examine the rs4311 SNP in the ACE gene, previously implicated in panic a... | BeFree | 25921615 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000789.4(ACE):c.1488-58T>C AND not provided | ClinVar | Detail |
| ACE ID/DD genotypes in combination with ACE rs4311, rs4343, and AGT rs699 mutant genotypes increased... | DisGeNET | Detail |
| Here we examine the rs4311 SNP in the ACE gene, previously implicated in panic attacks, in the relat... | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs4311 dbSNP
- Genome
- hg19
- Position
- chr17:61,560,763-61,560,763
- Variant Type
- snv
- Reference Allele
- T
- 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))
- rs4311
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.6621
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 11097
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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