Variant #0000194129 (NC_000023.10:g.79269442A>C, NM_001109878.1:c.-947A>C (TBX22))
Chromosome |
X |
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.79269442A>C |
DNA change (hg38) |
g.80013943A>C |
Published as |
-815A>C |
ISCN |
- |
DB-ID |
TBX22_000034 See all 7 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs6523677 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Global Variome, with Curator vacancy |
Date created |
2011-11-21 23:46:52 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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