View genomic variant #0000017782

Chromosome 15
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.90628537G>A
Published as -
GERP -
Segregation -
DB-ID IDH2_000003
MSCV MSCV_0017782
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.04587 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
IDH2 00000831 NM_002168.2 0000017782 ./. - - c.1050C>T p.(=) - - - -
IDH2 00000830 XM_005254893.1 0000017782 ./. - - c.894C>T p.(=) - - - -
IDH2 00000829 XM_005254894.1 0000017782 ./. - - c.660C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000146092; RCV000534348; RCV000676984;
Chromosome 15:90628537..90628537
Allele frequencies from ESP 0.04587
Allele frequencies from ExAC 0.02934
Allele frequencies from TGP 0.09046
ClinVar Allele ID 169179
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0013345, MedGen:C3150909, OMIM:613657, Orphanet:79315|MedGen:CN169374
ClinVar preferred disease name not provided|D-2-hydroxyglutaric aciduria 2|not specified
HGVS variant names NC 000015.9:g.90628537G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA172285
Gene symbol:Gene id. IDH2:3418
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 11540478
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