Variant #0000007644 (NC_000004.11:-, KIT(NM_000222.2):c.1859T>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_00037 |
Frequency |
- |
Variant remarks |
the Val620Ala mutation is novel and may result in a previously undescribed phenotype
with melanocyte instability, leading to progressive loss of pigmentation as well as the progressive
appearance of the hyperpigmented macules |
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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