Variant #0000691899 (NC_000015.9:g.89825056A>G, NM_002693.2:c.*34926T>C (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.89825056A>G
DNA change (hg38) -
Published as FANCI(NM_001113378.1):c.1573A>G (p.M525V, p.(Met525Val))
ISCN -
DB-ID POLG_000123 See all 4 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) 0.00228 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-09-15 15:50:26 +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.1573A>G r.(?) p.(Met525Val) -
POLG NM_002693.2 -?/. - c.*34926T>C r.(=) p.(=) -


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