Colon Cancer: Gene >> GPS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306823
Start	82056692:82056692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1192G>A
AA Mutation	p.Ala398Thr(p.A398T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306823
Start	82054685:82054685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>A
AA Mutation	p.Asp166Asn(p.D166N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000306823
Start	82055220:82055220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750722265
CDS Mutation	c.758C>T
AA Mutation	p.Ala253Val(p.A253V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306823
Start	82056939:82056939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366C>T
AA Mutation	p.Arg456Trp(p.R456W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306823
Start	82053302:82053302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62T>G
AA Mutation	p.Val21Gly(p.V21G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306823
Start	82056076:82056076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.922C>T
AA Mutation	p.Arg308Cys(p.R308C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306823
Start	82054603:82054603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747792808
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306823
Start	82056530:82056530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108C>T
AA Mutation	p.Arg370Cys(p.R370C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript