Variant #0000727240 (NC_000019.9:g.33333233_33333236del, NC_000019.9(NM_001126335.1):c.1075-9_1075-6del (SLC7A9))
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.33333233_33333236del |
DNA change (hg38) |
- |
Published as |
SLC7A9(NM_001243036.1):c.1075-9_1075-6delTTCT |
ISCN |
- |
DB-ID |
SLC7A9_000041 |
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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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