Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAP3K7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90586835:90586835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Glu17Lys(p.E17K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90516568:90516568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1754A>G
AA Mutation	p.Tyr585Cys(p.Y585C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90544606:90544606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762121500
CDS Mutation	c.1237C>T
AA Mutation	p.Arg413Cys(p.R413C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369329
Start	90552175:90552175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369329
Start	90544613:90544613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1230G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369329
Start	90556603:90556603(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.504delG
AA Mutation	p.Thr169GlnfsTer3(p.T169Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369329
Start	90553567:90553567(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.627delA
AA Mutation	p.Lys209AsnfsTer14(p.K209Nfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369329
Start	90571731:90571731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197A>G
AA Mutation	p.Glu66Gly(p.E66G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369329
Start	90547271:90547271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1197C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000369329
Start	90548082:90548082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045G>T
AA Mutation	p.Glu349Ter(p.E349*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript