chr13:48349024:G>T Detail (hg38) (RB1)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr13:48,923,160-48,923,160 View the variant detail on this assembly version. |
| hg38 | chr13:48,349,024-48,349,024 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000321.2:c.607+1G>T | |
| Ensemble | ENST00000267163.6:c.607+1G>T | |
| ENST00000650461.1:c.607+1G>T |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
Pathogenic
|
2024-05-20 | criteria provided, multiple submitters, no conflicts | retinoblastoma |
germline
unknown
|
Detail |
|
Pathogenic
|
2022-08-24 | criteria provided, single submitter | not provided |
germline
|
Detail |
|
Pathogenic
|
2022-04-11 | criteria provided, single submitter | Hereditary cancer-predisposing syndrome |
germline
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.500 | retinoblastoma | NA | CLINVAR | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000321.3(RB1):c.607+1G>T AND Retinoblastoma | ClinVar | Detail |
| NM_000321.3(RB1):c.607+1G>T AND not provided | ClinVar | Detail |
| NM_000321.3(RB1):c.607+1G>T AND Hereditary cancer-predisposing syndrome | ClinVar | Detail |
| NA | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs587776789 dbSNP
- Genome
- hg38
- Position
- chr13:48,349,024-48,349,024
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
Genome browser