Variant #0000004109 (NC_000023.10:-, GLA(NM_000169.2):c.?)
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
c.1149_1150insA, c.1152delC |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
GLA_00008 See all 31 reported entries |
| Frequency |
- |
| Variant remarks |
- |
| ClassClinical |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Qi Ming |
| Database submission license |
No license selected |
| Created by |
Qi Ming |
Variant on transcripts
|