Colon Cancer: Gene >> MAP2K6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000590474
Start	69519345:69519345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>T
AA Mutation	p.Gln93His(p.Q93H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000590474
Start	69505789:69505789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26G>A
AA Mutation	p.Arg9Gln(p.R9Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000590474
Start	69523528:69523528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550A>G
AA Mutation	p.Asn184Asp(p.N184D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000590474
Start	69519418:69519418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352G>A
AA Mutation	p.Ala118Thr(p.A118T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590474
Start	69519429:69519429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590474
Start	69526653:69526653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367955676
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000590474
Start	69517548:69517548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753824437
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Ter(p.R61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000590474
Start	69505788:69505788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25C>T
AA Mutation	p.Arg9Ter(p.R9*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000590474
Start	69516854:69516854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MAP2K6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000590474
Start	69520372:69520372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469A>G
AA Mutation	p.Lys157Glu(p.K157E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000590474
Start	69517521:69517521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.154G>T
AA Mutation	p.Asp52Tyr(p.D52Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000590474
Start	69516871:69516871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>T
AA Mutation	p.Asp34Tyr(p.D34Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590474
Start	69520365:69520365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462C>A
Mutation Classification	Silent
Feature Type	Transcript