chr13:49027168:C>T Detail (hg19) (RB1)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr13:49,027,168-49,027,168 |
| hg38 | chr13:48,453,032-48,453,032 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000321.2:c.1735C>T | NP_000312.2:p.Arg579Ter |
| Ensemble | ENST00000267163.6:c.1735C>T | ENST00000267163.6:p.Arg579Ter |
| ENST00000650461.1:c.1735C>T | ENST00000650461.1:p.Arg579Ter |
Summary
MGeND
| Clinical significance |
not provided
|
| Variant entry | 3 |
| GWAS entry | |
| Disease area statistics | Show details |
Disease area statistics
MGeND
| Clinical significance | Last evaluated | Condition | Origin | Submission ID | Submitter | Institute | Citation | Comment | Image |
|---|---|---|---|---|---|---|---|---|---|
|
not provided
|
bronchus or lung, unspecified |
not provided
|
MGS000042
(TMGS000093) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
|
not provided
|
descending colon |
not provided
|
MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan | ||||
|
not provided
|
bronchus or lung, unspecified |
not provided
|
MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan |
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
Pathogenic
|
2024-05-20 | criteria provided, multiple submitters, no conflicts | retinoblastoma |
de novo
germline
somatic
|
Detail |
|
Pathogenic
|
2019-01-09 | criteria provided, single submitter | Hereditary cancer-predisposing syndrome |
germline
|
Detail |
|
Pathogenic
|
2020-02-25 | criteria provided, single submitter | not provided |
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.1735C>T (p.Arg579Ter) AND Retinoblastoma | ClinVar | Detail |
| NM_000321.3(RB1):c.1735C>T (p.Arg579Ter) AND Hereditary cancer-predisposing syndrome | ClinVar | Detail |
| NM_000321.3(RB1):c.1735C>T (p.Arg579Ter) AND not provided | 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
- rs121913305 dbSNP
- Genome
- hg19
- Position
- chr13:49,027,168-49,027,168
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
Genome browser