Variant #0000699533 (NC_000009.11:g.135820608C>T, NM_000368.4:c.-822G>A (TSC1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135820608C>T |
DNA change (hg38) |
g.132945221C>T |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_000533 See all 2 reported entries |
Variant remarks |
common variant in 5' upstream region; HGVS nomenclature = NG_012386.1:g.4413G>A |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs4962083 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
MnlI- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Rosemary Ekong |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Rosemary Ekong |
Date created |
2020-11-02 10:52:17 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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