Genomic variant #0000108669

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.857099C>T
Reference dbSNP
DB-ID LINC01128_000004
Frequency 0.973
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     
LINC01128 NR_047519.1 ./. - n.4429C>T - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arraySNP - 905346 Admin