Colon Cancer: Gene >> SST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287641
Start	187669135:187669135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746348246
CDS Mutation	c.281C>T
AA Mutation	p.Pro94Leu(p.P94L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287641
Start	187669114:187669114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302G>A
AA Mutation	p.Arg101His(p.R101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287641
Start	187669153:187669153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263G>T
AA Mutation	p.Arg88Ile(p.R88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287641
Start	187670247:187670248(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.44_45insTA
AA Mutation	p.Val16ThrfsTer68(p.V16Tfs*68)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SST

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287641
Start	187670256:187670256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36G>A
Mutation Classification	Silent
Feature Type	Transcript