Variant #0000557308 (NC_000016.9:g.2138432C>T, NC_000016.9(NM_000548.3):c.5260-15C>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.2138432C>T |
| DNA change (hg38) |
g.2088431C>T |
| Published as |
PKD1(NM_001009944.3):c.*1296G>A, TSC2(NM_000548.3):c.5260-15C>T, TSC2(NM_000548.5):c.5260-15C>T |
| ISCN |
- |
| DB-ID |
TSC2_000338 See all 9 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) |
0.00153 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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