Variant #0000015037 (NC_000023.10:-, TAZ(NM_000116.3):c.280C>A)
Chromosome |
X |
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 |
TAZ_00037 |
Frequency |
- |
Variant remarks |
another patient with a missense mutation at the same position (R94C) has been previously reported
(Johnston et al. 1997). These data suggest that R94S is not
a common polymorphism, but a disease-causing 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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