Colon Cancer: Gene >> KITLG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228280
Start	88516385:88516385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Ala157Thr(p.A157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228280
Start	88516467:88516467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228280
Start	88545764:88545764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551116470
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228280
Start	88516479:88516479(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.375delA
AA Mutation	p.Lys125AsnfsTer31(p.K125Nfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228280
Start	88507118:88507119(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.623dupC
AA Mutation	p.Gly209TrpfsTer41(p.G209Wfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KITLG

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228280
Start	88518778:88518778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282C>A
Mutation Classification	Silent
Feature Type	Transcript