chr15:89333747:C>G Detail (hg38) (POLG, POLGARF)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr15:89,876,978-89,876,978 View the variant detail on this assembly version. |
hg38 | chr15:89,333,747-89,333,747 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001126131.1:c.8G>C | NP_001119603.1:p.Arg3Pro |
NM_002693.2:c.8G>C | NP_002684.1:p.Arg3Pro | |
Ensemble | ENST00000268124.11:c.8G>C | ENST00000268124.11:p.Arg3Pro |
Type | Transcript | Protein |
---|---|---|
RefSeq | ||
Ensemble | ENST00000706918.1:c.63G>C | ENST00000706918.1:p.Pro21= |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2001-07-01 | no assertion criteria provided | Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1 |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.481 | PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_002693.3(POLG):c.8G>C (p.Arg3Pro) AND Progressive external ophthalmoplegia with mitochondrial DNA... | 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
- rs121918045 dbSNP
- Genome
- hg38
- Position
- chr15:89,333,747-89,333,747
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- G
Genome browser