Variant #0000989361 (NC_000015.9:g.89876442C>G, NM_002693.2:c.544G>C (POLG))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.89876442C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID POLG_000293
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs768242927
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-03 19:50:02 +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     
POLG NM_002693.2 ?/. - c.544G>C r.(?) p.(Gly182Arg)


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