Colon Cancer: Gene >> TRAF3IP2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000340026
Start	111575645:111575645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1226T>G
AA Mutation	p.Leu409Trp(p.L409W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111575647:111575647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1224A>T
AA Mutation	p.Glu408Asp(p.E408D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111572917:111572917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1295T>C
AA Mutation	p.Leu432Ser(p.L432S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111591837:111591837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376682410
CDS Mutation	c.277C>T
AA Mutation	p.Arg93Cys(p.R93C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111592041:111592041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73C>A
AA Mutation	p.Pro25Thr(p.P25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000340026
Start	111559456:111559457(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1673dupA
AA Mutation	p.Tyr558Ter(p.Y558*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000340026
Start	111591637:111591639(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.475_477delCCT
AA Mutation	p.Pro159del(p.P159del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRAF3IP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111567673:111567673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337G>T
AA Mutation	p.Arg446Ile(p.R446I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111562985:111562985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1558C>G
AA Mutation	p.Leu520Val(p.L520V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111559534:111559534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1596G>T
AA Mutation	p.Trp532Cys(p.W532C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111591836:111591836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141777182
CDS Mutation	c.278G>A
AA Mutation	p.Arg93His(p.R93H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340026
Start	111591912:111591912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202G>T
AA Mutation	p.Asp68Tyr(p.D68Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript