Colon Cancer: Gene >> HPGD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296522
Start	174491969:174491969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788C>G
AA Mutation	p.Ala263Gly(p.A263G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296522
Start	174518073:174518073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296522
Start	174522049:174522050(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.111_112insC
AA Mutation	p.Asn38GlnfsTer3(p.N38Qfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296522
Start	174522051:174522052(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.109dupT
AA Mutation	p.Trp37LeufsTer4(p.W37Lfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HPGD

No Mutation Annotation!