Variant #0000297221 (NC_000015.9:g.89876858_89876860dup, NM_002693.2:c.156_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.89876858_89876860dup
DNA change (hg38) g.89333627_89333629dup
Published as POLG(NM_001126131.1):c.150_152dup (p.(Gln53dup)), POLG(NM_002693.2):c.156_158dupGCA (p.Q55dup), POLG(NM_002693.3):c.125delGinsGGCA (p.Q55dup), POLG...
ISCN -
DB-ID POLG_000102 See all 5 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.*17168_*17170dup r.(=) p.(=) -
POLG NM_002693.2 -/. - c.156_158dup r.(?) p.(Gln55dup) -


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