Variant #0000317224 (NC_000009.11:g.135781078_135781081del, NM_000368.4:c.1888_1891del (TSC1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135781078_135781081del |
DNA change (hg38) |
g.132905691_132905694del |
Published as |
TSC1(NM_000368.4):c.1888_1891delAAAG (p.K630Qfs*22) |
ISCN |
- |
DB-ID |
TSC1_000116 See all 60 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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-09-15 15:50:26 +02:00 (CEST) |

Variant on transcripts
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