Colon Cancer: Gene >> TCP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321394
Start	159784835:159784835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501C>A
AA Mutation	p.Phe167Leu(p.F167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321394
Start	159785486:159785486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370832633
CDS Mutation	c.388C>T
AA Mutation	p.Arg130Cys(p.R130C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321394
Start	159779643:159779643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1438C>T
AA Mutation	p.Arg480Cys(p.R480C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321394
Start	159779784:159779784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760874138
CDS Mutation	c.1297C>T
AA Mutation	p.Arg433Trp(p.R433W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321394
Start	159785988:159785988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289G>A
AA Mutation	p.Ala97Thr(p.A97T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321394
Start	159780476:159780476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064G>T
AA Mutation	p.Arg355Ile(p.R355I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000321394
Start	159780964:159780964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944A>G
AA Mutation	p.Asp315Gly(p.D315G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321394
Start	159779084:159779084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1632T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321394
Start	159784043:159784044(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.694dupG
AA Mutation	p.Ala232GlyfsTer7(p.A232Gfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TCP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321394
Start	159785432:159785432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321394
Start	159779770:159779770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767827941
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_lost
Transcription ID	ENST00000321394
Start	159779045:159779045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1671A>C
AA Mutation	p.Ter557CysextTer18(p.*557Cext*18)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript