Genomic variant #0000588806

Individual ID 00000001
Chromosome 15
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.85400336T>C
Reference -
DB-ID ALPK3_000037
dbSNP ID rs55727747
Frequency 0.005814
Allele Count 3
Allele Number 516
Combined Depth 9226
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00331 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALPK3 NM_020778.4 ./. - c.2973T>C r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin