Variant #0000064186 (NC_000002.11:g.167163663C>T, SCN9A(NM_002977.3):c.259-79G>A)

Individual ID 00036991
Chromosome 2
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.167163663C>T
DNA change (hg38) g.166307153C>T
Published as -
ISCN -
DB-ID SCN9A_000094
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs4447616
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Andreas Laner
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
SCN9A NM_002977.3 -/. - c.259-79G>A r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000037061 DNA SEQ - - SCN9A 1 Andreas Laner