Genomic variant #0000387121

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.133541910C>T
Reference -
DB-ID PRDM12_000001
dbSNP ID rs115102915
Frequency 0.009728
Allele Count 5
Allele Number 514
Combined Depth 2254
Homozygous -
Heterozygote -
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     
PRDM12 NM_021619.2 ./. - c.224-85C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin