Variant #0000011662 (NC_000001.10:-, NMNAT1(NM_022787.3):c.507G>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_00001 See all 4 reported entries |
Frequency |
- |
Variant remarks |
It is inherited from mother who carries the mutation p.W169X.
There are five members in this family. Only the daughter is the patient and has the mutations p.W169X and p.E257K. Her two normal bothers all carry the mutation p.W169X. The parents are normal. The mother only carries the mutation p.W169X. The father carries the mutation p.E257K. |
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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