Variant #0000064188 (NC_000002.11:g.167163372T>C, SCN9A(NM_002977.3):c.377+94A>G)

Individual ID 00036993
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.167163372T>C
DNA change (hg38) g.166306862T>C
Published as -
ISCN -
DB-ID SCN9A_000001 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs58349687
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.377+94A>G r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000037063 DNA SEQ - - SCN9A 1 Andreas Laner