Variant #0000469530 (NC_000009.11:g.135773001A[17-21], NM_000368.4:c.2626-4T[17_21] (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.135773001A[17-21] |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_000175 See all 3 reported entries |
Variant remarks |
five alleles of 17-21monomer T runs (18 Ts in reference sequence) |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
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 09:56:34 +01:00 (CET) |
Variant on transcripts
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