Genomic variant #0000420412

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.104855670G>A
Reference -
DB-ID NT5C2_000021
dbSNP ID rs1926029
Frequency 0.306
Allele Count 158
Allele Number 516
Combined Depth 5597
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.31985 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NT5C2 NM_012229.4 ./. - c.813+26C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin