Genomic variant #0000470871

Individual ID 00000001
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.65217854C>T
Reference dbSNP
DB-ID TECRL_000021
dbSNP ID rs1552210
Frequency 0.32264
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)     

Position     

RNA change     

Protein     
TECRL NM_001010874.4 ./. - c.286+23036G>A - - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904756 Admin