Colon Cancer: Gene >> CAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241052
Start	34452107:34452107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752948472
CDS Mutation	c.380G>A
AA Mutation	p.Arg127Gln(p.R127Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241052
Start	34468292:34468292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138694186
CDS Mutation	c.1331G>A
AA Mutation	p.Arg444Gln(p.R444Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241052
Start	34456048:34456048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778007071
CDS Mutation	c.749C>T
AA Mutation	p.Ala250Val(p.A250V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241052
Start	34461255:34461255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144190885
CDS Mutation	c.1061G>A
AA Mutation	p.Arg354His(p.R354H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241052
Start	34468356:34468356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1395C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241052
Start	34456052:34456052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201434009
CDS Mutation	c.753G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241052
Start	34456801:34456801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040C>G
AA Mutation	p.Pro347Arg(p.P347R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241052
Start	34468305:34468305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241052
Start	34456190:34456190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373984976
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript