Colon Cancer: Gene >> RIT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326695
Start	42743687:42743687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.460G>A
AA Mutation	p.Glu154Lys(p.E154K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326695
Start	42923599:42923599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326695
Start	42743667:42743667(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.480delT
AA Mutation	p.Phe160LeufsTer18(p.F160Lfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326695
Start	42743555:42743559(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.588_592delGAGAA
AA Mutation	p.Lys198GlnfsTer60(p.K198Qfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326695
Start	43115430:43115431(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs765499217
CDS Mutation	c.89dupG
AA Mutation	p.Val31SerfsTer3(p.V31Sfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RIT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326695
Start	42743674:42743674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199574261
CDS Mutation	c.473G>T
AA Mutation	p.Gly158Val(p.G158V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326695
Start	43115435:43115435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>T
AA Mutation	p.Gly29Trp(p.G29W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript