Genomic variant #0000000020

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.762273G>A
Reference -
DB-ID LINC00115_000007
dbSNP ID rs3115849
Frequency 0.764
Allele Count 394
Allele Number 516
Combined Depth 10242
Homozygous 151
Heterozygote 92
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.630C>T r.(?) -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin