Genomic variant #0000115516

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.167162450G>A
Reference -
DB-ID SCN9A_000113
dbSNP ID rs199609865
Frequency 0.001953
Allele Count 1
Allele Number 512
Combined Depth 2296
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00017 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN9A NM_002977.3 ./. - c.468-20C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin