Variant #0000722338 (NC_000009.11:g.135773000G>A, NC_000009.11(NM_000368.4):c.2626-3C>T (TSC1))
| Chromosome |
9 |
| 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.135773000G>A |
| DNA change (hg38) |
- |
| Published as |
TSC1(NM_000368.4):c.2626-3C>T, TSC1(NM_000368.4):c.2626-4_2626-3delTCinsTT, TSC1(NM_000368.5):c.2626-3C>T |
| ISCN |
- |
| DB-ID |
TSC1_000774 See all 6 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) |
Retrieve |
| 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 |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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