Colon Cancer: Gene >> STK11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326873
Start	1226603:1226603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762482152
CDS Mutation	c.1258G>T
AA Mutation	p.Ala420Ser(p.A420S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326873
Start	1226543:1226543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326873
Start	1223108:1223108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778274196
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326873
Start	1206958:1206958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs786201234
CDS Mutation	c.45C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326873
Start	1219345:1219345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs730881969
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326873
Start	1221315:1221315(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.842delC
AA Mutation	p.Pro281ArgfsTer6(p.P281Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326873
Start	1221314:1221315(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.842dupC
AA Mutation	p.Leu282AlafsTer3(p.L282Afs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	start_lost
Transcription ID	ENST00000326873
Start	1206914:1206914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STK11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326873
Start	1220467:1220467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.559G>T
AA Mutation	p.Gly187Cys(p.G187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript