Variant #0000126776 (NC_000011.9:g.22233066T>C, NC_000011.9(NM_213599.2):c.138+206T>C (ANO5))
Chromosome |
11 |
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.22233066T>C |
DNA change (hg38) |
g.22211520T>C |
Published as |
- |
ISCN |
- |
DB-ID |
ANO5_000010 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs4922981 |
Origin |
Germline |
Segregation |
- |
Frequency |
0.19-0.90 |
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 |
Johan den Dunnen |
Date created |
2010-02-14 22:37:07 +01:00 (CET) |
Date last edited |
2012-11-02 20:40:23 +01:00 (CET) |

Variant on transcripts
|