Colon Cancer: Gene >> TP53I3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238721
Start	24083083:24083083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208G>A
AA Mutation	p.Ala70Thr(p.A70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000238721
Start	24079560:24079560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763377588
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Ter(p.R234*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000238721
Start	24080855:24080856(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs770325453
CDS Mutation	c.582dupA
AA Mutation	p.Glu195ArgfsTer5(p.E195Rfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TP53I3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238721
Start	24080851:24080851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587A>G
AA Mutation	p.Asp196Gly(p.D196G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238721
Start	24079527:24079527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733G>A
AA Mutation	p.Asp245Asn(p.D245N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000238721
Start	24083028:24083028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263C>T
AA Mutation	p.Ala88Val(p.A88V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript