Variant #0000699612 (NC_000009.11:g.(135779842_135780967)_(135781527_135782117)del, NC_000009.11(NM_000368.4):c.(1438+1_1439-1)_(1997+1_1998-1)del (TSC1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(135779842_135780967)_(135781527_135782117)del |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_001378 See all 2 reported entries |
Variant remarks |
exon 15 deleted |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
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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