Colon Cancer: Gene >> MAPKAPK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551404
Start	111890096:111890096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753238884
CDS Mutation	c.1279C>T
AA Mutation	p.Arg427Trp(p.R427W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000551404
Start	111883663:111883663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745405567
CDS Mutation	c.743G>A
AA Mutation	p.Arg248Gln(p.R248Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000551404
Start	111870286:111870286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Trp(p.R137W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000551404
Start	111871091:111871091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490C>T
AA Mutation	p.Pro164Ser(p.P164S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000551404
Start	111842770:111842770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MAPKAPK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551404
Start	111883761:111883761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Val281Met(p.V281M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript