Variant #0000293272 (NC_000016.9:g.2096239G>A, NM_000548.3:c.-1857G>A (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2096239G>A |
DNA change (hg38) |
g.2046238G>A |
Published as |
NTHL1(NM_001318193.1):c.268C>T (p.(Gln90Ter)), NTHL1(NM_002528.7):c.244C>T (p.Q82*) |
ISCN |
- |
DB-ID |
NTHL1_000001 See all 23 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) |
0.00143 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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