Genomic variant #0000420428

Individual ID 00000001
Chromosome 10
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.104934709T>C
Reference -
DB-ID NT5C2_000037
dbSNP ID rs10883841
Frequency 0.101
Allele Count 52
Allele Number 516
Combined Depth 5665
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.1101 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NT5C2 NM_012229.4 ./. - c.7A>G r.(?) p.(Thr3Ala)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin