Variant #0000011665 (NC_000001.10:-, NMNAT1(NM_022787.3):c.817A>G)
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_00008 |
Frequency |
- |
Variant remarks |
It is inherited from father who carries the mutations p.N273D and p.L153V.
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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