View genomic variant #0000020050

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.41903957C>G
Published as -
GERP -
Segregation -
DB-ID ACO2_000001
MSCV MSCV_0020050
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 0000020050 ./. - - c.336C>G p.(Ser112Arg) - - - -
ACO2 00000020 XM_005261621.1 0000020050 ./. - - c.98-11C>G p.(=) - - - -
ACO2 00000019 XM_005261622.1 0000020050 ./. - - c.128+8136C>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000022421;
Chromosome 22:41903957..41903957
ClinVar Allele ID 38538
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.41903957C>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:CA128476|OMIM:100850.0001|UniProtKB:Q99798#VAR 067543
Gene symbol:Gene id. ACO2:50
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 786200924
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