Variant #0000011656 (NC_000001.10:-, NMNAT1(NM_022787.3):c.451G>T)

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_00004
Frequency -
Variant remarks Only the patient's sample was available. The patient has mutations p.E257K and p.V151F.
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.451G>T - p.Val151Phe