Colon Cancer: Gene >> ICAM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000412356
Start	64003686:64003686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607A>G
AA Mutation	p.Ile203Val(p.I203V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000412356
Start	64005325:64005325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110C>T
AA Mutation	p.Ala37Val(p.A37V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000412356
Start	64002818:64002818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565156038
CDS Mutation	c.757C>T
AA Mutation	p.Arg253Cys(p.R253C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000412356
Start	64003680:64003680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613C>T
AA Mutation	p.His205Tyr(p.H205Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000412356
Start	64003736:64003736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758140513
CDS Mutation	c.557G>A
AA Mutation	p.Arg186His(p.R186H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000412356
Start	64006638:64006638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000412356
Start	64002861:64002861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202007015
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ICAM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000412356
Start	64003709:64003709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584A>G
AA Mutation	p.Asp195Gly(p.D195G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript