Variant #0000452969 (NC_000001.10:g.156837936C>T, NM_002529.3:c.469C>T (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.156837936C>T |
DNA change (hg38) |
g.156868144C>T |
Published as |
- |
ISCN |
- |
DB-ID |
NTRK1_000115 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs141629165 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-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 10:41:44 +01:00 (CET) |
Date last edited |
2019-01-19 15:40:28 +01:00 (CET) |

Variant on transcripts
|