Variant #0000566835 (NC_000019.9:g.33353427C>T, NM_001126335.1:c.544G>A (SLC7A9))
Chromosome |
19 |
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.33353427C>T |
DNA change (hg38) |
g.32862521C>T |
Published as |
SLC7A9(NM_001243036.1):c.544G>A (p.A182T), SLC7A9(NM_014270.5):c.544G>A (p.(Ala182Thr), p.A182T) |
ISCN |
- |
DB-ID |
SLC7A9_000032 See all 6 reported entries |
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) |
0.00257 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|