Variant #0000782301 (NC_000016.9:g.2098578G>C, NC_000016.9(NM_000548.3):c.-29-10G>C (TSC2))
Chromosome |
16 |
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.2098578G>C |
DNA change (hg38) |
g.2048577G>C |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_003022 See all 7 reported entries |
Variant remarks |
variant in intron 1 |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs28537973 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
505/304440 alleles, 4 homozygotes |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00075 View details |
Owner |
Rosemary Ekong |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Rosemary Ekong |
Date created |
2021-05-04 16:22:13 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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