Genomic variant #0000000021

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.762320C>T
Reference -
DB-ID LINC00115_000008
dbSNP ID rs75333668
Frequency 0.025
Allele Count 13
Allele Number 516
Combined Depth 10297
Homozygous 1
Heterozygote 11
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.583G>A r.(?) -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin