View genomic variant #0000026895
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
Type |
- |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17355139T>G |
Published as |
- |
GERP |
- |
Segregation |
- |
DB-ID |
chr1_000440 |
MSCV |
- |
dbSNP ID |
- |
Frequency |
- |
Sources |
; |
Reference |
- |
Variant remarks |
- |
Genetic origin |
- |
Variant_disease |
- |
Average frequency (large NGS studies) |
Retrieve |
Owner |
Lishuang Shen |
Variant on transcripts
ClinVar @ MSeqDR | RCVaccession | RCV001064015; RCV003353144; | Chromosome | 1:17355139..17355139 | ClinVar Allele ID | 823003 | Disease database name and identifier | MONDO:MONDO:0007273, MedGen:C1861848, OMIM:115310, Orphanet:29072|Human Phenotype Ontology:HP:0002666, MONDO:MONDO:0008233, MedGen:C0031511, OMIM:171300, Orphanet:29072|Human Phenotype Ontology:HP:0100723, MONDO:MONDO:0011719, MeSH:D046152, MedGen:C0238198, OMIM:606764, Orphanet:44890|MONDO:MONDO:0015356, MeSH:D009386, MedGen:C0027672, Orphanet:140162 | ClinVar preferred disease name | Paragangliomas 4|Pheochromocytoma|Gastrointestinal stroma tumor|Hereditary cancer-predisposing syndrome | HGVS variant names | NC 000001.10:g.17355139T>C | ClinVar review status | criteria provided, conflicting interpretations | Clinical Significance | Conflicting interpretations of pathogenicity | Conflicting clinical significance | Likely pathogenic(1)|Uncertain significance(1) | Variant type | single nucleotide variant | Sequence Ontology for variant type | SO:0001483 | Gene symbol:Gene id. | SDHB:6390 | Molecular consequence | SO:0001583|missense variant | Allele origin | germline | dbSNP ID | 201372280 | Variant Flags | : |
ClinVar @ MSeqDR as full content XML tree
ClinVar @ MSeqDR | RCVaccession | RCV000457681; RCV000570298; RCV001755710; RCV002481485; RCV003476135; | Chromosome | 1:17355139..17355139 | ClinVar Allele ID | 390901 | Disease database name and identifier | MONDO:MONDO:0011740, MedGen:C1847319, OMIM:606864, Orphanet:97286|MONDO:MONDO:0030974, MedGen:C5543176, OMIM:619224|Human Phenotype Ontology:HP:0100723, MONDO:MONDO:0011719, MeSH:D046152, MedGen:C0238198, OMIM:606764, Orphanet:44890|MONDO:MONDO:0007273, MedGen:C1861848, OMIM:115310, Orphanet:29072|Human Phenotype Ontology:HP:0002666, MONDO:MONDO:0008233, MedGen:C0031511, OMIM:171300, Orphanet:29072|MONDO:MONDO:0015356, MeSH:D009386, MedGen:C0027672, Orphanet:140162|MedGen:C3661900 | ClinVar preferred disease name | Carney-Stratakis syndrome|Mitochondrial complex 2 deficiency, nuclear type 4|Gastrointestinal stroma tumor|Paragangliomas 4|Pheochromocytoma|Hereditary cancer-predisposing syndrome|not provided | HGVS variant names | NC 000001.10:g.17355139T>G | ClinVar review status | criteria provided, multiple submitters, no conflicts | Clinical Significance | Uncertain significance | Variant type | single nucleotide variant | Sequence Ontology for variant type | SO:0001483 | Variant clinical sources reported | ClinGen:CA16609924 | Gene symbol:Gene id. | SDHB:6390 | Molecular consequence | SO:0001583|missense variant | Allele origin | germline | dbSNP ID | 201372280 | Variant Flags | : |
ClinVar @ MSeqDR as full content XML tree
MSeqDR View Variant at Gbrowse Mitomap Mitochondrial Variant Phenotype Information:
None Ensembl Variant Phenotype Information:
None
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