Genomic variant #0000115519

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.167163043T>C
Reference -
DB-ID SCN9A_000116
dbSNP ID rs9646771
Frequency 0.672
Allele Count 347
Allele Number 516
Combined Depth 7989
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.71297 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN9A NM_002977.3 ./. - c.444A>G r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin