Variant #0000887125 (NC_000006.11:g.20402607_20402612dup, NM_001949.3:c.144_149dup (E2F3))

Chromosome 6
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.20402607_20402612dup
DNA change (hg38) -
Published as E2F3(NM_001949.5):c.144_149dupCGCCGC (p.A52_A53dup)
ISCN -
DB-ID E2F3_000002
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
E2F3 NM_001949.3 -/. - c.144_149dup r.(?) p.(Ala52_Ala53dup)


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