Variant #0000011660 (NC_000001.10:-, NMNAT1(NM_022787.3):c.769G>A)
Chromosome |
1 |
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 |
NMNAT1_00002 See all 9 reported entries |
Frequency |
- |
Variant remarks |
It may be inherited from father who carries the mutation p.E257K.
There are two patients in this family. The patients are brothers and have another normal sister. The patients have mutations p.W85X and p.E257K. The sister carries the mutation p.E257K. The parents are normal. Only maternal sample was available. The mother only carries the mutation p.W85X. |
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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