Variant #0001079068 (NC_000017.10:g.62481973G>A, NM_007215.3:c.982C>T (POLG2))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.62481973G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID POLG2_000012 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs782472762
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-06-29 17:13:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLG2 NM_007215.3 +?/. - c.982C>T r.(?) p.(Arg328Ter)


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