Colon Cancer: Gene >> TRAF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261464
Start	211356392:211356392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302G>T
AA Mutation	p.Arg101Ile(p.R101I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261464
Start	211372182:211372182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154C>T
AA Mutation	p.Ala385Val(p.A385V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261464
Start	211365430:211365430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Cys(p.R251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261464
Start	211360024:211360024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765593941
CDS Mutation	c.491G>T
AA Mutation	p.Arg164Leu(p.R164L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261464
Start	211372206:211372206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373368870
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393Gln(p.R393Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261464
Start	211361161:211361161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113925874
CDS Mutation	c.695C>T
AA Mutation	p.Thr232Met(p.T232M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261464
Start	211360764:211360764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.606T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261464
Start	211361105:211361105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261464
Start	211372576:211372576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1548C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000261464
Start	211360023:211360023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200980823
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Ter(p.R164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRAF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261464
Start	211369546:211369546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884T>C
AA Mutation	p.Phe295Ser(p.F295S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261464
Start	211372445:211372445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1417C>A
AA Mutation	p.Leu473Met(p.L473M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript