Genomic variant #0000387123

Individual ID 00000001
Chromosome 9
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.133541958C>T
Reference -
DB-ID PRDM12_000003
dbSNP ID rs199527715
Frequency 0.016
Allele Count 8
Allele Number 516
Combined Depth 5553
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00746 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRDM12 NM_021619.2 ./. - c.224-37C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin