Variant #0000306111 (NC_000015.9:g.89876693G>A, NM_002693.2:c.293C>T (POLG))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89876693G>A
DNA change (hg38) g.89333462G>A
Published as POLG(NM_002693.2):c.293C>T (p.A98V)
ISCN -
DB-ID POLG_000091
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.*17003G>A r.(=) p.(=) -
POLG NM_002693.2 -?/. - c.293C>T r.(?) p.(Ala98Val) -


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