Variant #0000004599 (NC_000016.9:g.2122286_2122301delTGAGTCCCTGCGCTAT, TSC2(NM_000548.3):c.2142_2157delTGAGTCCCTGCGCTAT)
Individual ID |
00004599 |
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2122286_2122301delTGAGTCCCTGCGCTAT |
Reference |
- |
DB-ID |
TSC2_000075 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
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