View genomic variant #0000000613

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.90631935G>C
Published as -
GERP 3.650
Segregation -
DB-ID IDH2_000002 See all 2 reported entries
MSCV MSCV_0000613
dbSNP ID rs267606870
Frequency -
Sources ; clinVar; Ensembl;
Reference 20847235
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 0000000613 +/+ - 4/11 c.418C>G p.(Arg140Gly) probably_damaging(1) missense_variant - deleterious(0)
IDH2 00000830 XM_005254893.1 0000000613 +/+ - 4/11 c.262C>G p.(Arg88Gly) probably_damaging(1) missense_variant - deleterious(0)
IDH2 00000829 XM_005254894.1 0000000613 +/+ - 2/9 c.28C>G p.(Arg10Gly) probably_damaging(1) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000422389; RCV000421344; RCV000428106; RCV000438361; RCV000438997; RCV001796031;
Chromosome 15:90631935..90631935
ClinVar Allele ID 362868
Disease database name and identifier Human Phenotype Ontology:HP:0006775, MONDO:MONDO:0009693, MeSH:D009101, MedGen:C0026764, OMIM:254500, Orphanet:29073, Orphanet:85443|Human Phenotype Ontology:HP:0100834, MONDO:MONDO:0005335, MeSH:D015179, MedGen:C0009404|MedGen:CN517202|MONDO:MONDO:0010150, MeSH:D000077195, MedGen:C1168401, OMIM:275355, Orphanet:67037|MONDO:MONDO:0018881, MeSH:D009190, MedGen:C3463824, OMIM:614286, Orphanet:52688|Human Phenotype Ontology:HP:0001914, Human Phenotype Ontology:HP:0004808, Human Phenotype Ontology:HP:0004843, Human Phenotype Ontology:HP:0005516, Human Phenotype Ontology:HP:0006724, Human Phenotype Ontology:HP:0006728, MONDO:MONDO:0018874, MeSH:D015470, MedGen:C0023467, OMIM:601626, Orphanet:519
ClinVar preferred disease name Multiple myeloma|Neoplasm of the large intestine|not provided|Squamous cell carcinoma of the head and neck|Myelodysplastic syndrome|Acute myeloid leukemia
HGVS variant names NC 000015.9:g.90631935G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16602464|Genetic Testing Registry (GTR):GTR000559520
Gene symbol:Gene id. IDH2:3418
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 267606870
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000015832;
Chromosome 15:90631935..90631935
ClinVar Allele ID 29756
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.90631935G>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA124281|Genetic Testing Registry (GTR):GTR000559520|OMIM:147650.0002
Gene symbol:Gene id. IDH2:3418
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 267606870
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