chr15:89326965:C>T Detail (hg38) (POLG, POLGARF)

Information

Genome

Assembly Position
hg19 chr15:89,870,196-89,870,196 View the variant detail on this assembly version.
hg38 chr15:89,326,965-89,326,965

HGVS

Type Transcript Protein
RefSeq NM_001126131.1:c.1532G>A NP_001119603.1:p.Ser511Asn
NM_002693.2:c.1532G>A NP_002684.1:p.Ser511Asn
Ensemble ENST00000268124.11:c.1532G>A ENST00000268124.11:p.Ser511Asn
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 174763 OMIM
HGNC 9179 HGNC
Ensembl ENSG00000140521 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2007-04-01 no assertion criteria provided Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.360 Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_002693.3(POLG):c.1532G>A (p.Ser511Asn) AND Progressive external ophthalmoplegia with mitochondria... ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs121918055 dbSNP
Genome
hg38
Position
chr15:89,326,965-89,326,965
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Genome browser