Variant #0000557332 (NC_000016.9:g.2141913G>A, NM_000548.3:c.*3302G>A (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.2141913G>A |
DNA change (hg38) |
g.2091912G>A |
Published as |
PKD1(NM_000296.3):c.11409-6C>T (p.(=)), PKD1(NM_001009944.2):c.11412-6C>T |
ISCN |
- |
DB-ID |
NTHL1_000182 |
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) |
0.0005 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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