Variant #0000469588 (NC_000009.11:g.135786839C>T, NC_000009.11(NM_000368.4):c.1029+1G>A (TSC1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic (dominant) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135786839C>T |
DNA change (hg38) |
g.132911452C>T |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_000062 See all 9 reported entries |
Variant remarks |
donor splice site affected; retention of intron 10 results in the addition of 113 amino acids |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs118203485 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
1/251294 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 |
2019-03-15 13:22:37 +01:00 (CET) |
Date last edited |
2020-11-02 09:57:30 +01:00 (CET) |

Variant on transcripts
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