Genomic variant #0000675239

Individual ID 00000001
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.75277611A>C
Reference -
DB-ID SEPT9_000002
dbSNP ID rs8070026
Frequency 0.128
Allele Count 66
Allele Number 516
Combined Depth 9338
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.10803 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEPT9 NM_001113491.1 ./. - c.-7A>C r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin