Colon Cancer: Gene >> KREMEN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303746
Start	2966706:2966706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551G>A
AA Mutation	p.Arg184His(p.R184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303746
Start	2967953:2967953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747033806
CDS Mutation	c.1322C>T
AA Mutation	p.Ala441Val(p.A441V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303746
Start	2966363:2966363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543637592
CDS Mutation	c.400C>T
AA Mutation	p.Pro134Ser(p.P134S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303746
Start	2966743:2966743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303746
Start	2967599:2967599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KREMEN2

No Mutation Annotation!