Variant #0000556096 (NC_000015.9:g.89876855_89876860dup, NM_002693.2:c.153_158dup (POLG))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89876855_89876860dup
DNA change (hg38) g.89333624_89333629dup
Published as POLG(NM_002693.2):c.141_146dupGCAGCA (p.(Gln48_Gln49dup)), POLG(NM_002693.2):c.147_152dupGCAGCA (p.Q54_Q55dup), POLG(NM_002693.2):c.153_158dupGCAGC...
ISCN -
DB-ID POLG_000110 See all 4 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.*17165_*17170dup r.(=) p.(=) -
POLG NM_002693.2 -?/. - c.153_158dup r.(?) p.(Gln54_Gln55dup) -


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