Variant #0000301123 (NC_000015.9:g.89873489C>G, NM_002693.2:c.678G>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.89873489C>G
DNA change (hg38) g.89330258C>G
Published as POLG(NM_002693.2):c.678G>C (p.Q226H), POLG(NM_002693.3):c.678G>C (p.(Gln226His), p.Q226H)
ISCN -
DB-ID POLG_000089 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) 0.0004 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCI NM_001113378.1 -?/. - c.*13799C>G r.(=) p.(=) -
POLG NM_002693.2 -?/. - c.678G>C r.(?) p.(Gln226His) -


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