Variant #0000562715 (NC_000017.10:g.62492582C>T, NM_007215.3:c.505G>A (POLG2))

Chromosome 17
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.62492582C>T
DNA change (hg38) g.64496464C>T
Published as POLG2(NM_007215.4):c.505G>A (p.A169T)
ISCN -
DB-ID POLG2_000004 See all 2 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) 0.14982 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX5 NM_004396.3 -/. - c.*3459G>A r.(=) p.(=)
POLG2 NM_007215.3 -/. - c.505G>A r.(?) p.(Ala169Thr)


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