Colon Cancer: Gene >> TRIP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261884
Start	64400777:64400777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777959222
CDS Mutation	c.653G>A
AA Mutation	p.Arg218His(p.R218H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261884
Start	64397627:64397627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144113386
CDS Mutation	c.427G>A
AA Mutation	p.Val143Ile(p.V143I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261884
Start	64406393:64406393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143968963
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261884
Start	64409693:64409693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748995821
CDS Mutation	c.908G>A
AA Mutation	p.Arg303Gln(p.R303Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261884
Start	64394039:64394039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195A>C
AA Mutation	p.Glu65Asp(p.E65D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261884
Start	64387870:64387870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7G>A
AA Mutation	p.Val3Met(p.V3M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261884
Start	64393994:64393994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000261884
Start	64409617:64409617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761865592
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Ter(p.R278*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000261884
Start	64395397:64395397(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.272-1delG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TRIP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261884
Start	64387910:64387910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>T
AA Mutation	p.Cys16Phe(p.C16F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000261884
Start	64445024:64445024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1594G>T
AA Mutation	p.Glu532Ter(p.E532*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript