Colon Cancer: Gene >> AMBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265132
Start	114062752:114062752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369822351
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Trp(p.R204W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265132
Start	114074052:114074052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438T>G
AA Mutation	p.Ile146Met(p.I146M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265132
Start	114073004:114073004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477A>C
AA Mutation	p.Glu159Asp(p.E159D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265132
Start	114078179:114078179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375383797
CDS Mutation	c.31C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265132
Start	114078161:114078161(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.49delG
AA Mutation	p.Val17Ter(p.V17*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AMBP

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000265132
Start	114062731:114062731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>T
AA Mutation	p.Glu211Ter(p.E211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript