Variant #0000011658 (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. The son and daughter are the patients and have mutations p.M35T and p.E257K. The parents are normal. The mother only carries the mutation p.E257K. The father carries the mutation p.M35T. |
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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