View genomic variant #0000017771

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.89876861C>T
Published as -
GERP -
Segregation -
DB-ID POLG_000270
MSCV MSCV_0017771
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

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 0000017771 ./. - - c.125G>A p.(Arg42Gln) - - - -
POLG 00000267 NM_002693.2 0000017771 ./. - - c.125G>A p.(Arg42Gln) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000545670; RCV000676334; RCV001847824; RCV003401026;
Chromosome 15:89876861..89876861
Allele frequencies from ExAC 0.00029
ClinVar Allele ID 203063
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0019064, MedGen:C0037773, OMIM:PS303350, Orphanet:685|MONDO:MONDO:0008758, MedGen:C0205710, OMIM:203700, Orphanet:726|.
ClinVar preferred disease name not provided|Hereditary spastic paraplegia|Progressive sclerosing poliodystrophy|POLG-related condition
HGVS variant names NC 000015.9:g.89876861C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(3)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA316606
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 74382477
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