Genomic variant #0000043665

Individual ID 00022096
Chromosome 10
Allele Both (homozygous)
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.72358577G>A
Reference -
DB-ID PRF1_000042 See all 63 reported entries
dbSNP ID rs885822
Variant remarks -
Genetic origin -
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Retrieve
Average frequency in greek population 0.01593
Allele Count 94
Allele Number 5900
Owner Stevi Xera
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRF1 NM_001083116.1 ./. - c.900C>T r.(=) p.(=)
PRF1 NM_005041.4 ./. - c.900C>T r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000007594 DNA SEQ-NG-I 1 - 37 Stevi Xera