Variant #0000007621 (NC_000004.11:-, KIT(NM_000222.2):c.1255_1257delGAC)
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Deletion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
KIT_00027 See all 2 reported entries |
Frequency |
- |
Variant remarks |
extracellular juxtamembrane domain encoded by exon 8 is a functional area capable of regulating KIT activity and establishes this deletion as a regulatory-type mutation.imatinib was able to inhibit KIT activation caused by this mutation, |
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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