Colon Cancer: Gene >> MAPK11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330651
Start	50267276:50267276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428C>T
AA Mutation	p.Ser143Leu(p.S143L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330651
Start	50270279:50270279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14G>A
AA Mutation	p.Arg5His(p.R5H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330651
Start	50266288:50266288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Cys(p.R234C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330651
Start	50265421:50265421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146256858
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330651
Start	50267830:50267830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236A>C
AA Mutation	p.Lys79Thr(p.K79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330651
Start	50267935:50267935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131C>T
AA Mutation	p.Ala44Val(p.A44V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript