Variant #0000981693 (NC_000016.9:g.2110765C>T, NM_000548.3:c.1070C>T (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2110765C>T |
DNA change (hg38) |
- |
Published as |
TSC2(NM_000548.3):c.1070C>T (p.A357V, p.(Ala357Val)), TSC2(NM_000548.5):c.1070C>T (p.A357V), TSC2(NM_001114382.2):c.1070C>T (p.A357V) |
ISCN |
- |
DB-ID |
TSC2_002016 See all 12 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00045 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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