Colon Cancer: Gene >> SNX10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338523
Start	26364587:26364587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164G>A
AA Mutation	p.Arg55Lys(p.R55K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338523
Start	26365069:26365069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.239delA
AA Mutation	p.Asn80ThrfsTer6(p.N80Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338523
Start	26365078:26365078(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.248delT
AA Mutation	p.Phe83SerfsTer3(p.F83Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338523
Start	26371990:26371991(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.481_482insGCTCTGT
AA Mutation	p.Glu161GlyfsTer10(p.E161Gfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SNX10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338523
Start	26364593:26364593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170T>G
AA Mutation	p.Phe57Cys(p.F57C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript