Variant #0000456168 (NC_000009.11:g.135776261G>A, NC_000009.11(NM_000368.4):c.2503-37C>T (TSC1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Probably does not affect function |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135776261G>A |
DNA change (hg38) |
g.132900874G>A |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_000935 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs756392360 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
2/143210 alleles |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
Rosemary Ekong |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Rosemary Ekong |
Date created |
2019-02-14 10:55:34 +01:00 (CET) |
Date last edited |
2020-11-02 09:57:30 +01:00 (CET) |

Variant on transcripts
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