View genomic variant #0000025138

Chromosome 15
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.89876558G>A
Published as -
GERP -
Segregation -
DB-ID POLG_000561
MSCV -
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 Lishuang Shen




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
POLG 00000266 NM_001126131.1 0000025138 ./. - - c.428C>T p.(Ala143Val) - - - -
POLG 00000267 NM_002693.2 0000025138 ./. - - c.428C>T p.(Ala143Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000758269; RCV000779176; RCV000995420; RCV002288792;
Chromosome 15:89876558..89876558
ClinVar Allele ID 203045
Disease database name and identifier MedGen:C4763519|MedGen:C3661900|MONDO:MONDO:0008758, MedGen:C0205710, OMIM:203700, Orphanet:726|MONDO:MONDO:0011835, MedGen:C1843851, OMIM:607459, Orphanet:70595
ClinVar preferred disease name POLG-Related Spectrum Disorders|not provided|Progressive sclerosing poliodystrophy|Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
HGVS variant names NC 000015.9:g.89876558G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(5)|Likely pathogenic(2)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 796052899
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