Variant #0001026769 (NC_000016.9:g.85952145T>C, NM_002163.2:c.724T>C (IRF8))

Chromosome 16
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.85952145T>C
DNA change (hg38) -
Published as IRF8(NM_002163.2):c.724T>C (p.Y242H), IRF8(NM_002163.4):c.724T>C (p.Y242H)
ISCN -
DB-ID IRF8_000001 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) 0.00191 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +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     
IRF8 NM_002163.2 -?/. - c.724T>C r.(?) p.(Tyr242His)


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