Colon Cancer: Gene >> MAP2K3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000342679
Start	21298479:21298479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77066538
CDS Mutation	c.116C>T
AA Mutation	p.Thr39Ile(p.T39I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342679
Start	21313508:21313508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931G>T
AA Mutation	p.Ala311Ser(p.A311S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342679
Start	21304526:21304526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139594289
CDS Mutation	c.669G>C
AA Mutation	p.Met223Ile(p.M223I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000342679
Start	21304552:21304552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695C>A
AA Mutation	p.Ala232Asp(p.A232D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000342679
Start	21298879:21298879(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.124delC
AA Mutation	p.Arg42GlyfsTer24(p.R42Gfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342679
Start	21312224:21312224(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.862delC
AA Mutation	p.Gln288SerfsTer19(p.Q288Sfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000342679
Start	21300584:21300584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205G>T
AA Mutation	p.Glu69Ter(p.E69*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAP2K3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342679
Start	21302248:21302248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505A>T
AA Mutation	p.Ile169Phe(p.I169F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript