Variant #0000556047 (NC_000015.9:g.89868870G>A, NM_002693.2:c.1760C>T (POLG))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89868870G>A
DNA change (hg38) g.89325639G>A
Published as POLG(NM_002693.2):c.1760C>T (p.P587L), POLG(NM_002693.3):c.1760C>T (p.(Pro587Leu), p.P587L)
ISCN -
DB-ID POLG_000046 See all 19 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) 0.00153 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCI NM_001113378.1 +/. - c.*9180G>A r.(=) p.(=) -
POLG NM_002693.2 +/. - c.1760C>T r.(?) p.(Pro587Leu) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.