Variant #0000452978 (NC_000001.10:g.156844766C>G, NM_002529.3:c.1320C>G (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.156844766C>G |
| DNA change (hg38) |
g.156874974C>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
NTRK1_000124 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs147443162 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00011 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 11:11:35 +01:00 (CET) |
| Date last edited |
2019-01-19 15:40:28 +01:00 (CET) |

Variant on transcripts
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