Variant #0000681739 (NC_000021.8:g.45716325C>A, NM_000383.3:c.1563C>A (AIRE))

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45716325C>A
DNA change (hg38) -
Published as AIRE(NM_000383.4):c.1563C>A (p.S521R)
ISCN -
DB-ID AIRE_000556
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIRE NM_000383.3 ?/. - c.1563C>A r.(?) p.(Ser521Arg)
PFKL NM_002626.4 ?/. - c.-3664C>A r.(?) p.(=)


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