Variant #0000007620 (NC_000004.11:-, KIT(NM_000222.2):c.2T>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_00028 |
| Frequency |
- |
| Variant remarks |
The second mutation was a novel change, 2T>C,
which affects the T of the ATG initiation codon
M1T and is likely to result in absence of translation
initiation |
| 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
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