Variant #0000965701 (NC_000010.10:g.27333132_27333133dup, NC_000010.10(NM_014915.2):c.1986-4_1986-3dup (ANKRD26))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.27333132_27333133dup |
| DNA change (hg38) |
- |
| Published as |
ANKRD26(NM_014915.2):c.1986-4_1986-3dupTT, ANKRD26(NM_014915.3):c.1986-4_1986-3dup, ANKRD26(NM_014915.3):c.1986-4_1986-3dupTT |
| ISCN |
- |
| DB-ID |
ANKRD26_000052 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) |
Retrieve |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2024-02-26 20:06:56 +01:00 (CET) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|