View genomic variant #0000017749

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.89876656G>A
Published as -
GERP -
Segregation -
DB-ID POLG_000245
MSCV MSCV_0017749
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
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 0000017749 ./. - - c.330C>T p.(=) - - - -
POLG 00000267 NM_002693.2 0000017749 ./. - - c.330C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000540376; RCV000591767;
Chromosome 15:89876656..89876656
Allele frequencies from ESP 0.00008
ClinVar Allele ID 464606
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.89876656G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA274566083
Gene symbol:Gene id. POLG:5428|POLGARF:125316803
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 376266682
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