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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NMNAT1 NM_022787.3 ./. 05 c.817A>G - p.Asn273Asp