Variant #0000854238 (NC_000015.9:g.89873460G>A, NM_002693.2:c.707C>T (POLG))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.89873460G>A
DNA change (hg38) -
Published as POLG(NM_002693.2):c.707C>T (p.T236I)
ISCN -
DB-ID POLG_000245
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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.*13770G>A r.(=) p.(=) -
POLG NM_002693.2 ?/. - c.707C>T r.(?) p.(Thr236Ile) -


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