Variant #0000864147 (NC_000015.9:g.89837139G>T, NM_002693.2:c.*22843C>A (POLG))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89837139G>T
DNA change (hg38) -
Published as FANCI(NM_001113378.1):c.2367G>T (p.(=))
ISCN -
DB-ID POLG_000236
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) 0.02432 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCI NM_001113378.1 -/. - c.2367G>T r.(?) p.(Ala789=) -
POLG NM_002693.2 -/. - c.*22843C>A r.(=) p.(=) -


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