View genomic variant #0000020051

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.41911862G>A
Published as -
GERP -
Segregation -
DB-ID ACO2_000002
MSCV MSCV_0020051
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     
ACO2 00000021 NM_001098.2 0000020051 ./. - - c.776G>A p.(Gly259Asp) - - - -
ACO2 00000020 XM_005261621.1 0000020051 ./. - - c.527G>A p.(Gly176Asp) - - - -
ACO2 00000019 XM_005261622.1 0000020051 ./. - - c.129-2678G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000169732;
Chromosome 22:41911862..41911862
ClinVar Allele ID 187200
Disease database name and identifier MONDO:MONDO:0013802, MedGen:C3281192, OMIM:614559, Orphanet:313850
ClinVar preferred disease name Infantile cerebellar-retinal degeneration
HGVS variant names NC 000022.10:g.41911862G>A
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:CA199206|OMIM:100850.0004|UniProtKB:Q99798#VAR 073436
Gene symbol:Gene id. ACO2:50
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 786204828
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