Colon Cancer: Gene >> MAPKAPK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367103
Start	206729073:206729073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367103
Start	206730008:206730008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782149296
CDS Mutation	c.601G>A
AA Mutation	p.Ala201Thr(p.A201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367103
Start	206685493:206685493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264G>T
AA Mutation	p.Glu88Asp(p.E88D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367103
Start	206730710:206730710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714G>T
AA Mutation	p.Glu238Asp(p.E238D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367103
Start	206729404:206729404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772956044
CDS Mutation	c.493G>A
AA Mutation	p.Glu165Lys(p.E165K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367103
Start	206728790:206728790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAPKAPK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367103
Start	206728794:206728794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364G>T
AA Mutation	p.Asp122Tyr(p.D122Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367103
Start	206729404:206729404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772956044
CDS Mutation	c.493G>A
AA Mutation	p.Glu165Lys(p.E165K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript