Genomic variant #0000811082

Individual ID 00000001
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.24536956A>G
Reference -
DB-ID PDK3_000012
dbSNP ID rs1487021665
Frequency 0.006897
Allele Count 2
Allele Number 290
Combined Depth 948
Homozygous 0
Heterozygote 2
Average frequency (large NGS studies) Retrieve
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDK3 NM_005391.4 ./. - c.596-94A>G r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin