View genomic variant #0000002889

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.242707133A>G
Published as -
GERP 4.450
Segregation -
DB-ID D2HGDH_000002
MSCV MSCV_0002889
dbSNP ID rs121434362
Frequency -
Sources ; clinvar;
Reference 16037974
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
D2HGDH 00000692 NM_152783.3 0000002889 +/+ - 10/10 c.1315A>G p.(Asn439Asp) probably_damaging(0.957) missense_variant - deleterious(0.02)
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ClinVar @ MSeqDR

RCVaccession RCV000001930;
Chromosome 2:242707133..242707133
ClinVar Allele ID 16895
Disease database name and identifier MONDO:MONDO:0024554, MedGen:C3152055, OMIM:600721, Orphanet:79315
ClinVar preferred disease name D-2-hydroxyglutaric aciduria 1
HGVS variant names NC 000002.11:g.242707133A>G
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:CA115238|OMIM:609186.0005|UniProtKB:Q8N465#VAR 025893
Gene symbol:Gene id. D2HGDH:728294
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 121434362
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