Colon Cancer: Gene >> KCNJ11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339994
Start	17387566:17387566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201264306
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Cys(p.R176C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339994
Start	17387430:17387430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662G>T
AA Mutation	p.Arg221Leu(p.R221L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339994
Start	17387905:17387905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339994
Start	17387786:17387786(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.306delC
AA Mutation	p.Ser103AlafsTer27(p.S103Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339994
Start	17387687:17387687(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.405delG
AA Mutation	p.Arg136AlafsTer3(p.R136Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KCNJ11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339994
Start	17387151:17387151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145935651
CDS Mutation	c.941G>A
AA Mutation	p.Arg314His(p.R314H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	start_lost
Transcription ID	ENST00000339994
Start	17388091:17388091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript