Variant #0000609961 (NC_000006.11:g.121629173_121629174del, NM_152730.4:c.642_643del (TBC1D32))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.121629173_121629174del |
| DNA change (hg38) |
g.121308027_121308028del |
| Published as |
TBC1D32(NM_152730.5):c.642_643delCT (p.C215Rfs*11), TBC1D32(NM_152730.6):c.642_643delCT (p.C215Rfs*11) |
| ISCN |
- |
| DB-ID |
TBC1D32_000020 See all 2 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 |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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