Variant #0000011663 (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 is inherited from mother who carries the mutation p.E257K. There are four members in this family. One son is the patient and has the mutations p.E257K, p.L153V and p.N273D. His normal brother carries the mutations p.L153V and p.N273D. The parents are normal. The mother only carries the mutation p.E257K. The father carries the mutations p.L153V and p.N273D. |
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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