View genomic variant #0000002547

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.89876751G>A
Published as -
GERP 4.130
Segregation -
DB-ID POLG_000054
MSCV MSCV_0002547
dbSNP ID -
Frequency -
Sources ; POLG_MUT_DB;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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 0000002547 +?/+? - 2/23 c.235C>T p.(Leu79Phe) probably_damaging(0.999) missense_variant - deleterious(0.01)
POLG 00000267 NM_002693.2 0000002547 +?/+? - 2/23 c.235C>T p.(Leu79Phe) probably_damaging(0.999) missense_variant - deleterious(0.01)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003317827;
Chromosome 15:89876751..89876751
ClinVar Allele ID 2738435
Disease database name and identifier MedGen:CN169374
ClinVar preferred disease name not specified
HGVS variant names NC 000015.9:g.89876751G>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
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