Variant #0000691907 (NC_000015.9:g.89876852_89876860dup, NM_002693.2:c.150_158dup (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.89876852_89876860dup
DNA change (hg38) -
Published as POLG(NM_002693.2):c.150_158dupGCAGCAGCA (p.Q53_Q55dup), POLG(NM_002693.3):c.150_158dupGCAGCAGCA (p.Q53_Q55dup)
ISCN -
DB-ID POLG_000178 See all 3 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) 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCI NM_001113378.1 -/. - c.*17162_*17170dup r.(=) p.(=) -
POLG NM_002693.2 -/. - c.150_158dup r.(?) p.(Gln53_Gln55dup) -


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