Variant #0000011661 (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 father who carries the mutation p.E257K.

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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NMNAT1 NM_022787.3 ./. 05 c.769G>A - p.Glu257Lys