Colon Cancer: Gene >> IK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000417647
Start	140655873:140655873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682C>T
AA Mutation	p.Arg228Trp(p.R228W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000417647
Start	140659025:140659025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538502414
CDS Mutation	c.1037G>A
AA Mutation	p.Arg346His(p.R346H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000417647
Start	140654042:140654042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509T>G
AA Mutation	p.Leu170Arg(p.L170R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000417647
Start	140659315:140659315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177C>T
AA Mutation	p.Pro393Ser(p.P393S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000417647
Start	140659103:140659103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746748598
CDS Mutation	c.1115G>A
AA Mutation	p.Arg372Gln(p.R372Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000417647
Start	140659333:140659333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195G>A
AA Mutation	p.Gly399Arg(p.G399R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000417647
Start	140654559:140654560(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.563_564insAA
AA Mutation	p.Met189ArgfsTer54(p.M189Rfs*54)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000417647
Start	140659048:140659048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758451409
CDS Mutation	c.1060C>T
AA Mutation	p.Arg354Cys(p.R354C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript