View genomic variant #0000017785

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.90633702C>A
Published as -
GERP -
Segregation -
DB-ID IDH2_000004
MSCV MSCV_0017785
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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 0000017785 ./. - - c.373+9G>T p.(=) - - - -
IDH2 00000830 XM_005254893.1 0000017785 ./. - - c.217+9G>T p.(=) - - - -
IDH2 00000829 XM_005254894.1 0000017785 ./. - - c.-17-1723G>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001395355;
Chromosome 15:90633702..90633702
Allele frequencies from ExAC 0.00003
ClinVar Allele ID 529160
Disease database name and identifier MONDO:MONDO:0013345, MedGen:C3150909, OMIM:613657, Orphanet:79315
ClinVar preferred disease name D-2-hydroxyglutaric aciduria 2
HGVS variant names NC 000015.9:g.90633702C>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA7733218
Gene symbol:Gene id. IDH2:3418
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 755607312
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