Variant #0000306120 (NC_000015.9:g.89861826T>C, NM_002693.2:c.3428A>G (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.89861826T>C
DNA change (hg38) g.89318595T>C
Published as POLG(NM_001126131.2):c.3428A>G (p.E1143G), POLG(NM_002693.2):c.3428A>G (p.E1143G), POLG(NM_002693.3):c.3428A>G (p.E1143G)
ISCN -
DB-ID POLG_000001 See all 11 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) 0.02875 View details
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 2023-04-16 21:50:28 +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.*2136T>C r.(=) p.(=) -
POLG NM_002693.2 -/. - c.3428A>G r.(?) p.(Glu1143Gly) -


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