Variant #0000011372 (NC_000004.12:g.54727230C>T, KIT(NM_000222.3):c.1553C>T)
| Individual ID |
00004111 |
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| DNA change (genomic) (Relative to hg38 / GRCh38) |
g.54727230C>T |
| Reference |
- |
| DB-ID |
KIT_000004 |
| dbSNP ID |
- |
| Variant remarks |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Agostina Tardivo-Instituto Fleming |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Instituto Nacional del Cancer |

Variant on transcripts
Screenings
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