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 International |
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) |

Variant on transcripts
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