Colon Cancer: Gene >> TRAF3IP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367024
Start	209775403:209775403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829A>C
AA Mutation	p.Asn277His(p.N277H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367024
Start	209760112:209760112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759256006
CDS Mutation	c.73C>T
AA Mutation	p.Arg25Cys(p.R25C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367024
Start	209760079:209760079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755111399
CDS Mutation	c.40C>T
AA Mutation	p.Arg14Trp(p.R14W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367024
Start	209775666:209775666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983A>G
AA Mutation	p.Asp328Gly(p.D328G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367024
Start	209778169:209778169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1248G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367024
Start	209777408:209777408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000367024
Start	209782068:209782068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576C>T
AA Mutation	p.Arg526Ter(p.R526*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRAF3IP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367024
Start	209772963:209772963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718G>T
AA Mutation	p.Asp240Tyr(p.D240Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript