Colon Cancer: Gene >> CABLES2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279101
Start	62391364:62391364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181T>C
AA Mutation	p.Val394Ala(p.V394A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279101
Start	62396384:62396384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371230015
CDS Mutation	c.458C>T
AA Mutation	p.Pro153Leu(p.P153L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000279101
Start	62391323:62391323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143971422
CDS Mutation	c.1222G>A
AA Mutation	p.Ala408Thr(p.A408T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000279101
Start	62391092:62391092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1316G>A
AA Mutation	p.Arg439Gln(p.R439Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279101
Start	62396332:62396332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202000885
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CABLES2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279101
Start	62392433:62392433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047G>T
AA Mutation	p.Arg349Ser(p.R349S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript