Genomic variant #0000515725

Individual ID 00000001
Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.121659917G>A
Reference -
DB-ID P2RX4_000031
dbSNP ID rs25642
Frequency 0.05
Allele Count 26
Allele Number 516
Combined Depth 11060
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.03775 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
P2RX4 NM_001256796.1 ./. - c.423G>A r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin