Variant #0000981016 (NC_000014.8:g.77493668_77493676del, NM_024496.3:c.480_488del (IRF2BPL))

Chromosome 14
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.77493668_77493676del
DNA change (hg38) -
Published as IRF2BPL(NM_024496.4):c.480_488del (p.(Ala162_Ala164del)), IRF2BPL(NM_024496.4):c.480_488delCGCCGCCGC (p.A162_A164del)
ISCN -
DB-ID IRF2BPL_000045 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.480_488del r.(?) p.(Ala162_Ala164del)


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