Colon Cancer: Gene >> MAPK8IP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329492
Start	50603662:50603662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329492
Start	50603488:50603488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437T>C
AA Mutation	p.Leu146Pro(p.L146P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329492
Start	50606982:50606982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2294G>A
AA Mutation	p.Arg765His(p.R765H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329492
Start	50606736:50606736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2203A>G
AA Mutation	p.Lys735Glu(p.K735E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000329492
Start	50605064:50605064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770751117
CDS Mutation	c.1765A>G
AA Mutation	p.Ser589Gly(p.S589G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329492
Start	50605039:50605039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1740C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329492
Start	50605850:50605850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2040G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329492
Start	50603878:50603878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749260984
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK8IP2

No Mutation Annotation!