Colon Cancer: Gene >> GGCT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275428
Start	30497185:30497185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474G>T
AA Mutation	p.Glu158Asp(p.E158D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275428
Start	30498888:30498888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>A
AA Mutation	p.Ala113Glu(p.A113E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275428
Start	30498823:30498823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403C>A
AA Mutation	p.Pro135Thr(p.P135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GGCT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275428
Start	30500545:30500545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776460145
CDS Mutation	c.278C>A
AA Mutation	p.Ser93Tyr(p.S93Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript