View genomic variant #0000025165

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.89876916G>A
Published as -
GERP -
Segregation -
DB-ID POLG_000562
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 0000025165 ./. - - c.70C>T p.(Arg24Cys) - - - -
POLG 00000267 NM_002693.2 0000025165 ./. - - c.70C>T p.(Arg24Cys) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000758484;
Chromosome 15:89876916..89876916
ClinVar Allele ID 610807
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.89876916G>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 1196273210
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001219852;
Chromosome 15:89876916..89876916
ClinVar Allele ID 927455
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.89876916G>T
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 1196273210
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