View genomic variant #0000025137

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.89876555T>C
Published as -
GERP -
Segregation -
DB-ID POLG_000560
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 0000025137 ./. - - c.431A>G p.(Gln144Arg) - - - -
POLG 00000267 NM_002693.2 0000025137 ./. - - c.431A>G p.(Gln144Arg) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000758339; RCV002312323; RCV001838125; RCV002499301;
Chromosome 15:89876555..89876555
ClinVar Allele ID 579960
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0024528, MedGen:C1834846, OMIM:157640|MONDO:MONDO:0009783, MedGen:C4225153, OMIM:258450, Orphanet:254886|MONDO:MONDO:0013350, MedGen:C3150914, OMIM:613662, Orphanet:298|MONDO:MONDO:0008758, MedGen:C0205710, OMIM:203700, Orphanet:726|MONDO:MONDO:0011283, MedGen:C4551995, OMIM:603041, Orphanet:298|MONDO:MONDO:0011835, MedGen:C1843851, OMIM:607459, Orphanet:70595|MedGen:C3661900
ClinVar preferred disease name Inborn genetic diseases|Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1|Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1|Mitochondrial DNA depletion syndrome 4b|Progressive sclerosing poliodystrophy|Mitochondrial DNA depletion syndrome 1|Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis|not provided
HGVS variant names NC 000015.9:g.89876555T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
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 1056580076
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