Variant #0001017388 (NC_000011.9:g.22294441C>G, NM_213599.2:c.2141C>G (ANO5))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.22294441C>G |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ANO5_000060 See all 21 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs200631556 |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00087 View details |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2024-11-18 16:38:01 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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