Colon Cancer: Gene >> LRRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296144
Start	46521608:46521608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980G>A
AA Mutation	p.Gly327Asp(p.G327D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000296144
Start	46521656:46521656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932T>C
AA Mutation	p.Phe311Ser(p.F311S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000296144
Start	46519062:46519062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068A>T
AA Mutation	p.Glu356Asp(p.E356D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296144
Start	46527527:46527527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296144
Start	46545250:46545250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LRRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296144
Start	46545225:46545225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752406824
CDS Mutation	c.154G>A
AA Mutation	p.Glu52Lys(p.E52K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296144
Start	46551568:46551568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146344015
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000296144
Start	46532889:46532889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>T
AA Mutation	p.Glu171Ter(p.E171*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript