View genomic variant #0000025169

Chromosome 15
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.90645600A>G
Published as -
GERP -
Segregation -
DB-ID IDH2_000005
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00067 View details
Owner Lishuang Shen




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 0000025169 ./. - - c.23T>C p.(Val8Ala) - - - -
IDH2 00000830 XM_005254893.1 0000025169 ./. - - c.-1834T>C p.(=) - - - -
IDH2 00000829 XM_005254894.1 0000025169 ./. - - c.-110T>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000676986; RCV000690494;
Chromosome 15:90645600..90645600
Allele frequencies from ESP 0.00067
Allele frequencies from ExAC 0.00013
Allele frequencies from TGP 0.00220
ClinVar Allele ID 550029
Disease database name and identifier MONDO:MONDO:0013345, MedGen:C3150909, OMIM:613657, Orphanet:79315|MedGen:C3661900
ClinVar preferred disease name D-2-hydroxyglutaric aciduria 2|not provided
HGVS variant names NC 000015.9:g.90645600A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. IDH2:3418|IDH2-DT:105370966
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 369445642
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