Genomic variant #0000115496

Individual ID 00000001
Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.167144995T>C
Reference -
DB-ID SCN9A_000093
dbSNP ID rs13402180
Frequency 0.352
Allele Count 181
Allele Number 514
Combined Depth 2178
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.38657 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN9A NM_002977.3 ./. - c.1266A>G r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin