View genomic variant #0000025129

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.89876340del
Published as -
GERP -
Segregation -
DB-ID POLG_000552
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 0000025129 ./. - - c.646del p.(Ser216Profs*50) - - - -
POLG 00000267 NM_002693.2 0000025129 ./. - - c.646del p.(Ser216Profs*50) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001986384;
Chromosome 15:89876339..89876339
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 1508476
Disease database name and identifier MONDO:MONDO:0008758, MedGen:C0205710, OMIM:203700, Orphanet:726
ClinVar preferred disease name Progressive sclerosing poliodystrophy
HGVS variant names NC 000015.9:g.89876339G>A
ClinVar review status criteria provided, single submitter
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 763592738
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000688138;
Chromosome 15:89876340..89876340
ClinVar Allele ID 573580
Disease database name and identifier MONDO:MONDO:0008758, MedGen:C0205710, OMIM:203700, Orphanet:726
ClinVar preferred disease name Progressive sclerosing poliodystrophy
HGVS variant names NC 000015.9:g.89876340del
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 1567193844
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