Variant #0000863692 (NC_000014.8:g.77493671_77493676dup, NM_024496.3:c.483_488dup (IRF2BPL))

Chromosome 14
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.77493671_77493676dup
DNA change (hg38) -
Published as IRF2BPL(NM_024496.4):c.477_482dupCGCCGC (p.A163_A164dup), IRF2BPL(NM_024496.4):c.483_488dupCGCCGC (p.A163_A164dup)
ISCN -
DB-ID IRF2BPL_000060 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRF2BPL NM_024496.3 -?/. - c.483_488dup r.(?) p.(Ala163_Ala164dup)


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