Variant #0000557338 (NC_000016.9:g.2142501C>T, NM_000548.3:c.*3890C>T (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2142501C>T |
DNA change (hg38) |
g.2092500C>T |
Published as |
PKD1(NM_000296.3):c.11246G>A (p.(Arg3749Gln)) |
ISCN |
- |
DB-ID |
PKD1_000466 See all 4 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 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
|