Genomic variant #0000000035

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.762637G>T
Reference -
DB-ID LINC00115_000022
dbSNP ID rs543295788
Frequency 0.005882
Allele Count 3
Allele Number 510
Combined Depth 2239
Homozygous 1
Heterozygote 1
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.266C>A r.(?) -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin