TP53 exon 5 frequency of known variants in Moroccan prostate cancer patients and their corresponding effects according to NCBI 1000 Genomes Browser and Human Genome Variation Society (HGVS) nomenclature

EffectVariant IDCDS changeGenome locationProtein changeFrequency, N = 48
Insertionrs786202525c.532_533insCCCChr17:7675079p.Pro177_His178insPro1 (2%)
Missensers1057519977c.423C>GChr17:7675189p.Cys141Trp9 (19%)
Missensers1131691037c.392A>TChr17:7675220p.Asn131Ile5 (10%)
Missensers138729528c.523C>GChr17:7675089p.Arg175Gly5 (10%)
Missensers1555526335c.377A>GChr17:7675235p.Tyr126Cys4 (8%)
Missensers758781593c.408A>CChr17:7675204p.Gln136His4 (8%)
Missensers1555526226c.439G>AChr17:7675173p.Val147Ile1 (2%)
Missensers28934875c.412G>CChr17:7675200p.Ala138Pro1 (2%)
Missensers587782596c.541C>AChr17:7675071p.Arg181Ser1 (2%)
Missensers730881999c.380C>GChr17:7675232p.Ser127Cys1 (2%)
Missensers786203071c.431A>CChr17:7675181p.Gln144Pro1 (2%)
NArs1321881901c.559+31G>AChr17:7675022NA26 (54%)
NArs1032547645c.559+22G>AChr17:7675031NA3 (6.25%)
NArs1221388024c.376-4A>TChr17:7675240NA1 (2%)
NArs1466952182c.376-51C>TChr17:7675287NA1 (2%)
NArs775915220c.559+8G>AChr17:7675045NA1 (2%)
NArs786202799c.376-2A>GChr17:7675238NA1 (2%)
Nonseners757274881c.430C>TChr17:7675182p.Gln144Ter1 (2%)
Synonymousrs786203928c.433C>TChr17:7675179p.Leu145=2 (4%)
Synonymousrs1131691034c.492G>AChr17:7675120p.Lys164=1 (2%)
Synonymousrs761222871c.468C>TChr17:7675144p.Arg156=1 (2%)
Synonymousrs876659481c.456G>AChr17:7675156p.Pro152=1 (2%)

CDS: coding DNA sequences