Colon Cancer: Gene >> LAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275635
Start	74219770:74219770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161G>C
AA Mutation	p.Gly54Ala(p.G54A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275635
Start	74219776:74219776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781903165
CDS Mutation	c.167G>A
AA Mutation	p.Arg56Gln(p.R56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275635
Start	74216063:74216063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369438020
CDS Mutation	c.88C>T
AA Mutation	p.Arg30Cys(p.R30C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275635
Start	74219990:74219990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369645558
CDS Mutation	c.209C>T
AA Mutation	p.Ala70Val(p.A70V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275635
Start	74224709:74224709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LAT2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275635
Start	74221676:74221676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript