Variant #0000324283 (NC_000015.9:g.89876989_89876992del, NM_002693.2:c.-3_1del (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.89876989_89876992del
DNA change (hg38) g.89333758_89333761del
Published as POLG(NM_002693.2):c.-3_1del (p.?)
ISCN -
DB-ID POLG_000113
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-07 09:22:21 +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.*17299_*17302del r.(=) p.(=) -
POLG NM_002693.2 ?/. - c.-3_1del r.(?) p.(Met1?) -


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