Variant #0000236467 (NC_000002.11:g.127827669G>C, NC_000002.11(NM_139343.2):c.316-3C>G (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.127827669G>C |
| DNA change (hg38) |
g.127070093G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BIN1_000036 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs113742431 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
? |
| 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 |
2010-12-28 11:40:11 +01:00 (CET) |
| Date last edited |
2012-11-02 20:40:23 +01:00 (CET) |

Variant on transcripts
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