Variant #0000658387 (NC_000018.9:g.45395766A>C, NM_005901.5:c.368T>G (SMAD2))
Chromosome |
18 |
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.45395766A>C |
DNA change (hg38) |
g.47869395A>C |
Published as |
SMAD2(NM_001003652.3):c.368T>G (p.(Leu123Trp)) |
ISCN |
- |
DB-ID |
SMAD2_000026 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|