Colon Cancer: Gene >> JAM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000480456
Start	25693833:25693833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319T>C
AA Mutation	p.Tyr107His(p.Y107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000480456
Start	25639865:25639865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44G>A
AA Mutation	p.Arg15His(p.R15H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000480456
Start	25698743:25698743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550982612
CDS Mutation	c.461G>A
AA Mutation	p.Arg154Gln(p.R154Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000480456
Start	25698801:25698801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000480456
Start	25693844:25693844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764021326
CDS Mutation	c.330A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> JAM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000480456
Start	25702221:25702221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649C>T
AA Mutation	p.Arg217Cys(p.R217C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript