Colon Cancer: Gene >> CUEDC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369937
Start	102423472:102423472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818C>T
AA Mutation	p.Ala273Val(p.A273V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369937
Start	102423472:102423472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.818C>G
AA Mutation	p.Ala273Gly(p.A273G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369937
Start	102423535:102423535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755T>C
AA Mutation	p.Val252Ala(p.V252A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369937
Start	102424329:102424329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199625253
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Trp(p.R116W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369937
Start	102424710:102424710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767718515
CDS Mutation	c.157G>A
AA Mutation	p.Asp53Asn(p.D53N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369937
Start	102424732:102424732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CUEDC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369937
Start	102423545:102423545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778175495
CDS Mutation	c.745G>A
AA Mutation	p.Asp249Asn(p.D249N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript