Genomic variant #0000000016

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.762061T>A
Reference -
DB-ID LINC00115_000003
dbSNP ID rs191348624
Frequency 0.016
Allele Count 8
Allele Number 516
Combined Depth 8394
Homozygous 0
Heterozygote 8
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LINC00115 NR_024321.1 ./. - n.842A>T r.(?) -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin