Variant #0001015897 (NC_000021.8:g.45705988T>C, NM_000383.3:c.99T>C (AIRE))
Chromosome |
21 |
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.45705988T>C |
DNA change (hg38) |
- |
Published as |
AIRE(NM_000383.2):c.99T>C (p.A33=), AIRE(NM_000383.4):c.99T>C (p.A33=) |
ISCN |
- |
DB-ID |
AIRE_000501 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) |
0.08987 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2024-10-29 21:08:56 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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