Variant #0000981499 (NC_000015.9:g.89865023C>T, NM_002693.2:c.2542G>A (POLG))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89865023C>T
DNA change (hg38) -
Published as POLG(NM_001126131.2):c.2542G>A (p.G848S), POLG(NM_002693.2):c.2542G>A (p.G848S), POLG(NM_002693.3):c.2542G>A (p.(Gly848Ser), p.G848S)
ISCN -
DB-ID POLG_000116 See all 14 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     

Haplotype     
FANCI NM_001113378.1 +/. - c.*5333C>T r.(=) p.(=) -
POLG NM_002693.2 +/. - c.2542G>A r.(?) p.(Gly848Ser) -


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