View genomic variant #0000026019

Chromosome 22
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.41903841C>G
Published as -
GERP -
Segregation -
DB-ID ACO2_000011
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00415 View details
Owner Lishuang Shen




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
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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 0000026019 ./. - - c.220C>G p.(Leu74Val) - - - -
ACO2 00000020 XM_005261621.1 0000026019 ./. - - c.9C>G p.(=) - - - -
ACO2 00000019 XM_005261622.1 0000026019 ./. - - c.128+8020C>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000169730; RCV000676884; RCV000764399; RCV000990458; RCV002292437;
Chromosome 22:41903841..41903841
Allele frequencies from ESP 0.00415
Allele frequencies from ExAC 0.00414
Allele frequencies from TGP 0.00160
ClinVar Allele ID 187198
Disease database name and identifier .|MONDO:MONDO:0013802, MedGen:C3281192, OMIM:614559, Orphanet:313850|MONDO:MONDO:0014571, MedGen:C4225384, OMIM:616289|MedGen:C3661900
ClinVar preferred disease name OPTIC ATROPHY 9, AUTOSOMAL RECESSIVE|Infantile cerebellar-retinal degeneration|Optic atrophy 9|not provided
HGVS variant names NC 000022.10:g.41903841C>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(4)|Benign(1)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA248785|OMIM:100850.0002|UniProtKB:Q99798#VAR 073435
Gene symbol:Gene id. ACO2:50
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 141772938
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