Skip to main content

Table 2 List of TP53 mutations identified in Rwandan gastric cancer patients

From: The spectrum of TP53 mutations in Rwandan patients with gastric cancer

Sample ID

Exon

/intron

Genomic

description

Coding DNA description

Protein Description

Effect

dbSNP_ID

GC090

Exon 4

g.7,676,060G>T

c.309C>A

p.Y103*

Nonsense

NA

GC057

Exon 4

g.7,676,055C>A

c.314G>T

p.G105V

Missense

NA

GC060

Exon 5

g.7,675,206del

c.406del

p.Q136Nfs*34

Frameshift

NA

GC028

Exon 5

g.7,675,185C>T

c.427G>A

p.V143M

Missense

rs587782620

GC021&

Exon 5

g.7,675,139_7,675,157del

c.459_477del

p.G154Wfs*10

Frameshift

NA

GC067

Exon 5

g.7,675,142A>G

c.470T>C

p.V157A

Missense

rs1131691023

GC019

Exon 5

g.7,675,139C>A

c.473G>T

p.R158L

Missense

rs587782144

GC014

Exon 5

g.7,675,138G>A

c.474C>T

p.Arg158=

Silent

rs139200646

GC053

Exon 5

g.7,675,094A>C

c.518T>G

p.V173G

Missense

rs1057519747

GC028

Exon 5

g.7,675,088C>T

c.524G>A

p.R175H

Missense

rs28934578

GC080

Exon 5

g.7,675,088C>T

c.524G>A

p.R175H

Missense

rs28934578

GC042

Exon 5

g.7,675,085C>A

c.527G>T

p.C176F

Missense

rs786202962

GC071

Exon 5

g.7,675,085C>A

c.527G>T

p.C176F

Missense

rs786202962

GC079

Exon 5

g.7,675,085C>A

c.527G>T

p.C176F

Missense

rs786202962

GC028

Exon 6

g.7,674,954G>A

c.577C>T

p.H193Y

Missense

rs876658468

GC075

Exon 6

g.7,674,950A>C

c.581T>G

p.L194R

Missense

rs1057519998

GC084

Exon 6

g.7,674,945G>A

c.586C>T

p.R196*

Nonsense

rs397516435

GC059

Exon 6

g.7,674,894G>A

c.637C>T

p.R213*

Nonsense

rs397516436

GC060

Exon 6

g.7,674,894G>A

c.637C>T

p.R213*

Nonsense

rs397516436

GC066

Exon 6

g.7,674,894G>A

c.637C>T

p.R213*

Nonsense

rs397516436

GC006

Exon 6

g.7,674,893C>A

c.638G>T

p.R213L

Missense

rs587778720

GC051

Exon 6

g.7,674,885C>T

c.646G>A

p.V216M

Missense

rs730882025

GC081

Exon 6

g.7,674,877del

c.654del

p.Y220Mfs*27

Frameshift

NA

GC038

Exon 7

g.7,674,230C>T

c.733G>A

p.G245S

Missense

rs28934575

GC067

Exon 7

g.7,674,230C>T

c.733G>A

p.G245S

Missense

rs28934575

GC014

Intron 7

g.7,674,180C>T

c.782+1G>A

p.?

Splice-site

NA

GC035

Exon 8

g.7,673,776G>C

c.844C>G

p.R282G

Missense

rs28934574

GC106

Exon 8

g.7,673,776G>A

c.844C>T

p.R282W

Missense

rs28934574

GC089

Exon 8

g.7,673,763T>A

c.857A>T

p.E286V

Missense

rs1057519985

  1. & newly identified variant, ID: identification, NA: Not applicable, g.: genomic, c.: coding, p.: protein, dbSNP: The Single Nucleotide Polymorphism Database, rs: The reference single nucleotide polymorphism