Variant #0000002477 (NC_000017.10:g.62034787G>A, SCN4A(NM_000334.4):c.2111C>T)

Individual ID 00002477
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.62034787G>A
Reference Saleem R1, Setty G, Khan A, Farrell D, Hussain N.(2013)
DB-ID SCN4A_000004
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
SCN4A NM_000334.4 ./. 13 c.2111C>T r.(?) p.(Thr704Met) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002477 ? ? SCN4A 1 Y Yang