chr1:161356841:G>A Detail (hg38) (SDHC)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr1:161,326,631-161,326,631 View the variant detail on this assembly version. |
| hg38 | chr1:161,356,841-161,356,841 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_001035511.1:c.242-5488G>A | |
| NM_003001.3:c.405+1G>A | ||
| NM_001035513.1:c.246+1G>A |
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 |
|---|---|---|---|---|---|
|
|
2011-01-04 | no assertion criteria provided | Carney-Stratakis syndrome |
|
Detail |
|
|
2011-01-04 | no assertion criteria provided | gastrointestinal stromal tumor |
|
Detail |
|
|
no assertion criteria provided | Carney triad |
|
Detail | |
|
|
no assertion criteria provided | Hereditary pheochromocytoma-paraganglioma |
|
Detail | |
|
|
2019-08-20 | criteria provided, single submitter | Paragangliomas 3,gastrointestinal stromal tumor |
|
Detail |
|
|
2019-08-20 | criteria provided, single submitter | Paragangliomas 3,gastrointestinal stromal tumor |
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.240 | Paragangliomas 3 | NA | CLINVAR | Detail | |
| 0.360 | PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA | NA | CLINVAR | Detail | |
| 0.121 | Carney triad | NA | CLINVAR | Detail | |
| 0.245 | Gastrointestinal Stromal Tumors | NA | CLINVAR | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_003001.5(SDHC):c.405+1G>A AND Carney-Stratakis syndrome | ClinVar | Detail |
| NM_003001.5(SDHC):c.405+1G>A AND Gastrointestinal stromal tumor | ClinVar | Detail |
| NM_003001.5(SDHC):c.405+1G>A AND Carney triad | ClinVar | Detail |
| NM_003001.5(SDHC):c.405+1G>A AND Hereditary pheochromocytoma-paraganglioma | ClinVar | Detail |
| NM_003001.5(SDHC):c.405+1G>A AND multiple conditions | ClinVar | Detail |
| NM_003001.5(SDHC):c.405+1G>A AND multiple conditions | ClinVar | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs587776653 dbSNP
- Genome
- hg38
- Position
- chr1:161,356,841-161,356,841
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
Genome browser
