Variant #0000236471 (NC_000002.11:g.127816536G>A, NC_000002.11(NM_139343.2):c.1002+51C>T (BIN1))
| Chromosome |
2 |
| 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.127816536G>A |
| DNA change (hg38) |
g.127058960G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BIN1_000033 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs2276580 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.00-0.15 |
| 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 |
2010-03-12 10:36:48 +01:00 (CET) |
| Date last edited |
2017-12-15 14:47:53 +01:00 (CET) |

Variant on transcripts
|