Genomic variant #0000033856

Individual ID 00017878
Chromosome 17
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.7576989_7576990dup
Reference -
DB-ID TP53_000014 See all 3 reported entries
dbSNP ID rs776692311
Variant remarks -
Genetic origin Germline
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Variant not found in online data sets
Average frequency in greek population 0.00052
Allele Count 3
Allele Number 5792
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 ?/? - c.919+29_919+30dup r.(=) p.(=)
TP53 NM_001126112.2 ?/? - c.919+29_919+30dup r.(=) p.(=)
TP53 NM_001126113.2 ?/? - c.919+29_919+30dup r.(=) p.(=)
TP53 NM_001126114.2 ?/? - c.919+29_919+30dup r.(=) p.(=)
TP53 NM_001126115.1 ?/? - c.523+29_523+30dup r.(=) p.(=)
TP53 NM_001126116.1 ?/? - c.523+29_523+30dup r.(=) p.(=)
TP53 NM_001126117.1 ?/? - c.523+29_523+30dup r.(=) p.(=)
TP53 NM_001126118.1 ?/? - c.802+29_802+30dup r.(=) p.(=)
TP53 NM_001276695.1 ?/? - c.802+29_802+30dup r.(=) p.(=)
TP53 NM_001276696.1 ?/? - c.802+29_802+30dup r.(=) p.(=)
TP53 NM_001276697.1 ?/? - c.442+29_442+30dup r.(=) p.(=)
TP53 NM_001276698.1 ?/? - c.442+29_442+30dup r.(=) p.(=)
TP53 NM_001276699.1 ?/? - c.442+29_442+30dup r.(=) p.(=)
TP53 NM_001276760.1 ?/? - c.802+29_802+30dup r.(=) p.(=)
TP53 NM_001276761.1 ?/? - c.802+29_802+30dup r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000001997 DNA SEQ-NG-I 1 - 12 Despoina Kalfakakou