chr19:55665483:A>G Detail (hg19) (TNNI3)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr19:55,665,483-55,665,483 |
| hg38 | chr19:55,154,115-55,154,115 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000363.4:c.464T>C | NP_000354.4:p.Met155Thr |
| Ensemble | ENST00000344887.10:c.464T>C | ENST00000344887.10:p.Met155Thr |
| ENST00000588882.1:c.389T>C | ENST00000588882.1:p.Met130Thr |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
| Clinical Significance |
Likely pathogenic
|
| Review star |  |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
Likely pathogenic
|
2011-06-16 | no assertion criteria provided | Primary dilated cardiomyopathy |
germline
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.360 | Cardiomyopathy, Dilated, 1FF | NA | CLINVAR | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000363.5(TNNI3):c.464T>C (p.Met155Thr) AND Primary dilated cardiomyopathy | ClinVar | Detail |
| NA | 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
- rs397516352 dbSNP
- Genome
- hg19
- Position
- chr19:55,665,483-55,665,483
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
Genome browser