Colon Cancer: Gene >> TOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358131
Start	44065914:44065914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542635212
CDS Mutation	c.1109C>T
AA Mutation	p.Ala370Val(p.A370V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358131
Start	43945926:43945926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14G>A
AA Mutation	p.Arg5His(p.R5H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358131
Start	44054473:44054473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853G>A
AA Mutation	p.Val285Met(p.V285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358131
Start	44054431:44054431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>A
AA Mutation	p.Ala271Thr(p.A271T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358131
Start	44054434:44054434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370568497
CDS Mutation	c.814G>A
AA Mutation	p.Ala272Thr(p.A272T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358131
Start	44051442:44051442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376494319
CDS Mutation	c.575G>A
AA Mutation	p.Arg192Gln(p.R192Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358131
Start	44066735:44066735(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1310delC
AA Mutation	p.Pro437ArgfsTer136(p.P437Rfs*136)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358131
Start	44065821:44065821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764077991
CDS Mutation	c.1016C>T
AA Mutation	p.Thr339Met(p.T339M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript