Variant #0000011648 (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. A son is the patient and has mutations p.W169X and p.E257K. He has an unaffected older brother. The parents are normal. The mother only carries the mutation p.E257K. The father carries the mutation p.W169X. |
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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