Genomic variant #0000588832

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.85403171C>T
Reference -
DB-ID ALPK3_000063
dbSNP ID rs150130260
Frequency 0.007752
Allele Count 4
Allele Number 516
Combined Depth 8895
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00023 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALPK3 NM_020778.4 ./. - c.4699+37C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin