Colon Cancer: Gene >> ST13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216218
Start	40835881:40835881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389T>C
AA Mutation	p.Leu130Pro(p.L130P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216218
Start	40835576:40835576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751496137
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Trp(p.R188W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216218
Start	40850834:40850834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Glu53Lys(p.E53K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216218
Start	40856520:40856520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216218
Start	40835868:40835868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216218
Start	40827160:40827160(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.917delG
AA Mutation	p.Gly306GlufsTer50(p.G306Efs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ST13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216218
Start	40848321:40848321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217G>A
AA Mutation	p.Glu73Lys(p.E73K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript