View genomic variant #0000025157

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.89876833C>T
Published as -
GERP -
Segregation -
DB-ID POLG_000398
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 0000025157 ./. - - c.153G>A p.(=) - - - -
POLG 00000267 NM_002693.2 0000025157 ./. - - c.153G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001365007;
Chromosome 15:89876833..89876834
ClinVar Allele ID 1049156
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.89876835 89876836insTTG
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Insertion
Sequence Ontology for variant type SO:0000667
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001821|inframe insertion
Allele origin germline
dbSNP ID 1466061893
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000676332; RCV000758501;
Chromosome 15:89876833..89876833
ClinVar Allele ID 550027
Disease database name and identifier MONDO:MONDO:0008758, MedGen:C0205710, OMIM:203700, Orphanet:726|MedGen:CN517202
ClinVar preferred disease name Progressive sclerosing poliodystrophy|not provided
HGVS variant names NC 000015.9:g.89876833C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 1453538834
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