View genomic variant #0000015786
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Probably does not affect function |
Type |
- |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43596058G>A |
Published as |
- |
GERP |
- |
Segregation |
- |
DB-ID |
RET_000012 |
MSCV |
MSCV_0015786 |
dbSNP ID |
- |
Frequency |
- |
Sources |
; clinvar; |
Reference |
- |
Variant remarks |
- |
Genetic origin |
- |
Variant_disease |
- |
Average frequency (large NGS studies) |
0.00046 View details |
Owner |
LOVD |
Variant on transcripts
ClinVar @ MSeqDR | RCVaccession | RCV000163611; RCV000200674; RCV000409943; RCV000412352; RCV000606849; RCV001105644; RCV001103697; RCV001105643; RCV001105642; | Chromosome | 10:43596058..43596058 | Allele frequencies from ESP | 0.00046 | Allele frequencies from ExAC | 0.00016 | Allele frequencies from TGP | 0.00020 | ClinVar Allele ID | 182944 | Disease database name and identifier | MONDO:MONDO:0017169, MedGen:C0027662, OMIM:PS131100, Orphanet:276161|MONDO:MONDO:0015356, MeSH:D009386, MedGen:C0027672, Orphanet:140162|MedGen:CN169374|MONDO:MONDO:0019003, MedGen:C4048306, Orphanet:653|MONDO:MONDO:0008082, MeSH:D018814, MedGen:C0025269, OMIM:162300, Orphanet:247709, Orphanet:653|MONDO:MONDO:0007723, MedGen:C3888239, OMIM:142623, Orphanet:388|MONDO:MONDO:0008234, MeSH:D018813, MedGen:C0025268, OMIM:171400, Orphanet:247698, Orphanet:653|MONDO:MONDO:0024519, MedGen:C1619700, OMIM:191830, Orphanet:411709|Human Phenotype Ontology:HP:0002666, MONDO:MONDO:0008233, MedGen:C0031511, OMIM:171300, Orphanet:29072 | ClinVar preferred disease name | Multiple endocrine neoplasia|Hereditary cancer-predisposing syndrome|not specified|Multiple endocrine neoplasia, type 2|Multiple endocrine neoplasia, type 2b|Hirschsprung disease, susceptibility to, 1|Multiple endocrine neoplasia, type 2a|Renal hypodysplasia/aplasia 1|Pheochromocytoma | HGVS variant names | NC 000010.10:g.43596058G>A | ClinVar review status | criteria provided, conflicting interpretations | Clinical Significance | Conflicting interpretations of pathogenicity | Conflicting clinical significance | Uncertain significance(1)|Benign(3)|Likely benign(6) | Variant type | single nucleotide variant | Sequence Ontology for variant type | SO:0001483 | Variant clinical sources reported | ClinGen:CA008616 | Gene symbol:Gene id. | RET:5979 | Molecular consequence | SO:0001627|intron variant, SO:0001819|synonymous variant | Allele origin | germline | dbSNP ID | 151267865 | Variant Flags | : |
ClinVar @ MSeqDR as full content XML tree
ClinVar @ MSeqDR | RCVaccession | RCV002443715; | Chromosome | 10:43596058..43596058 | ClinVar Allele ID | 1844666 | Disease database name and identifier | MONDO:MONDO:0015356, MeSH:D009386, MedGen:C0027672, Orphanet:140162 | ClinVar preferred disease name | Hereditary cancer-predisposing syndrome | HGVS variant names | NC 000010.10:g.43596058G>T | ClinVar review status | criteria provided, single submitter | Clinical Significance | Likely benign | Variant type | single nucleotide variant | Sequence Ontology for variant type | SO:0001483 | Gene symbol:Gene id. | RET:5979 | Molecular consequence | SO:0001627|intron variant, SO:0001819|synonymous variant | Allele origin | germline | 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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