Colon Cancer: Gene >> MAPK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52046600:52046600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>T
AA Mutation	p.Ala47Val(p.A47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52046560:52046560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>T
AA Mutation	p.Val34Phe(p.V34F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52061344:52061344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911G>A
AA Mutation	p.Arg304Gln(p.R304Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52046993:52046993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533T>C
AA Mutation	p.Met178Thr(p.M178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52050086:52050086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649G>A
AA Mutation	p.Ala217Thr(p.A217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52064450:52064450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616C>A
AA Mutation	p.Ser539Tyr(p.S539Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52046467:52046467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Glu3Lys(p.E3K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52058698:52058698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1049605
CDS Mutation	c.766C>T
AA Mutation	p.Arg256Cys(p.R256C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261845
Start	52064439:52064439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1605T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261845
Start	52050053:52050054(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.616_617delCC
AA Mutation	p.Pro206Ter(p.P206*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000261845
Start	52064689:52064690(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1855_1856insGCTTCTAA
AA Mutation	p.Val619GlyfsTer3(p.V619Gfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52064030:52064030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196G>A
AA Mutation	p.Arg399Gln(p.R399Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261845
Start	52064414:52064414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580T>C
AA Mutation	p.Phe527Ser(p.F527S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript