Variant #0000615107 (NC_000014.8:g.77493790_77493800del, NM_024496.3:c.336_346del (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.77493790_77493800del
DNA change (hg38) g.77027447_77027457del
Published as IRF2BPL(NM_024496.4):c.336_346delGCAGCAACAGC (p.Q113Afs*16)
ISCN -
DB-ID IRF2BPL_000021 See all 2 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRF2BPL NM_024496.3 -?/. - c.336_346del r.(?) p.(Gln113AlafsTer16)


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