Genomic variant #0000604348

Individual ID 00000001
Chromosome 16
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.8900241G>A
Reference -
DB-ID PMM2_000014
dbSNP ID rs62031146
Frequency 0.019
Allele Count 10
Allele Number 516
Combined Depth 7464
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.01439 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMM2 NM_000303.2 ./. - c.324G>A r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin