Variant #0000618389 (NC_000021.8:g.45711065_45711077del, NM_000383.3:c.967_979del (AIRE))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45711065_45711077del
DNA change (hg38) g.44291182_44291194del
Published as AIRE(NM_000383.2):c.967_979delCTGTCCCCTCCGC (p.L323Sfs*51), AIRE(NM_000383.3):c.967_979delCTGTCCCCTCCGC (p.(Leu323fs)), AIRE(NM_000383.4):c.967_979...
ISCN -
DB-ID AIRE_000079 See all 27 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIRE NM_000383.3 +/. - c.967_979del r.(?) p.(Leu323SerfsTer51)


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