Variant #0000401464 (NC_000016.9:g.2546553C>T, NM_001199107.1:c.404C>T (TBC1D24))
| Chromosome |
16 |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2546553C>T |
| DNA change (hg38) |
g.2496552C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TBC1D24_000076 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Somatic |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Jing Zhang |
| Database submission license |
No license selected |
| Created by |
Jing Zhang |
| Date created |
2018-08-19 13:58:10 +02:00 (CEST) |
| Date last edited |
2018-08-22 18:30:47 +02:00 (CEST) |

Variant on transcripts
Screenings
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