Variant #0000885865 (NC_000003.11:g.47043594_47043602del, NM_015175.2:c.4967_4975del (NBEAL2))
| Chromosome |
3 |
| 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.47043594_47043602del |
| DNA change (hg38) |
- |
| Published as |
NBEAL2(NM_015175.2):c.4948_4956del (p.(Ala1653_Ala1655del)), NBEAL2(NM_015175.2):c.4967_4975delCAGCTGCAG (p.A1656_A1658del) |
| ISCN |
- |
| DB-ID |
NBEAL2_000007 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 |
2022-11-01 13:01:21 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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