Genomic variant #0000115498

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.167145142A>G
Reference -
DB-ID SCN9A_000095
dbSNP ID rs13414203
Frequency 0.366
Allele Count 188
Allele Number 514
Combined Depth 3794
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.38516 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN9A NM_002977.3 ./. - c.1119T>C r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin