Variant #0000725541 (NC_000016.9:g.2142488C>G, NM_000548.3:c.*3877C>G (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2142488C>G |
DNA change (hg38) |
- |
Published as |
PKD1(NM_000296.3):c.11259G>C (p.(Leu3753=)), PKD1(NM_001009944.2):c.11262G>C (p.L3754=) |
ISCN |
- |
DB-ID |
PKD1_001438 See all 3 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) |
0.00494 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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