Variant #0000007586 (NC_000004.11:-, KIT(NM_000222.2):c.1676T>C)
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
KIT_00006 See all 6 reported entries |
| Frequency |
2/a family |
| Variant remarks |
The point mutation (VaP59~Ala) iden-
tified in our study is possibly a novel type of gain-of-
function mutation of c-kit, one that causes multiple
GISTs as well as cutaneous hyperpigmentation. |
| ClassClinical |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Qi Ming |
| Database submission license |
No license selected |
| Created by |
Qi Ming |

Variant on transcripts
|
|