Colon Cancer: Gene >> ILK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299421
Start	6608445:6608445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Pro103Ser(p.P103S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299421
Start	6609731:6609731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147558204
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299421
Start	6608154:6608154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299421
Start	6608049:6608049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56057203
CDS Mutation	c.93C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299421
Start	6608162:6608162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.211delC
AA Mutation	p.Leu71CysfsTer26(p.L71Cfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299421
Start	6608122:6608123(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs770182262
CDS Mutation	c.172dupG
AA Mutation	p.Ala58GlyfsTer11(p.A58Gfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ILK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299421
Start	6610180:6610180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759330457
CDS Mutation	c.1111C>T
AA Mutation	p.Arg371Cys(p.R371C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299421
Start	6608199:6608199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756301182
CDS Mutation	c.243T>C
Mutation Classification	Silent
Feature Type	Transcript