Variant #0000452973 (NC_000001.10:g.156837913C>A, NM_002529.3:c.446C>A (NTRK1))
| Chromosome |
1 |
| 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.156837913C>A |
| DNA change (hg38) |
g.156868121C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
NTRK1_000119 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs144609655 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2011-11-02 10:41:14 +01:00 (CET) |
| Date last edited |
2019-01-19 15:40:28 +01:00 (CET) |

Variant on transcripts
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