Colon Cancer: Gene >> MAP3K2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127308618:127308618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1601G>A
AA Mutation	p.Ser534Asn(p.S534N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127322073:127322073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376189453
CDS Mutation	c.1018G>A
AA Mutation	p.Val340Ile(p.V340I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127324179:127324179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740T>G
AA Mutation	p.Phe247Cys(p.F247C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127330472:127330472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298G>T
AA Mutation	p.Asp100Tyr(p.D100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127335915:127335915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219A>C
AA Mutation	p.Lys73Asn(p.K73N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127324215:127324215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704C>A
AA Mutation	p.Pro235His(p.P235H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127322104:127322104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.987G>T
AA Mutation	p.Arg329Ser(p.R329S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344908
Start	127338935:127338935(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.120delA
AA Mutation	p.Lys40AsnfsTer29(p.K40Nfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344908
Start	127326784:127326784(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.500delC
AA Mutation	p.Pro167GlnfsTer40(p.P167Qfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000344908
Start	127318222:127318222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776045361
CDS Mutation	c.1141G>T
AA Mutation	p.Glu381Ter(p.E381*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344908
Start	127322174:127322175(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.916_917insT
AA Mutation	p.His306LeufsTer6(p.H306Lfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127326754:127326754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530T>G
AA Mutation	p.Val177Gly(p.V177G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127324221:127324221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698G>A
AA Mutation	p.Arg233Gln(p.R233Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127323972:127323972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768G>T
AA Mutation	p.Glu256Asp(p.E256D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344908
Start	127329975:127329975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412G>T
AA Mutation	p.Asp138Tyr(p.D138Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript