Colon Cancer: Gene >> GPR31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366834
Start	167157822:167157822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10C>A
AA Mutation	p.Pro4Thr(p.P4T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366834
Start	167157525:167157525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>A
AA Mutation	p.Ala103Thr(p.A103T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366834
Start	167157815:167157815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201491639
CDS Mutation	c.17G>T
AA Mutation	p.Cys6Phe(p.C6F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366834
Start	167156908:167156908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924G>T
AA Mutation	p.Glu308Asp(p.E308D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366834
Start	167157582:167157582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777956303
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Cys(p.R84C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366834
Start	167157193:167157193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366834
Start	167157688:167157688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575627973
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000366834
Start	167156931:167156931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148093951
CDS Mutation	c.901C>T
AA Mutation	p.Arg301Ter(p.R301*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GPR31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366834
Start	167157618:167157618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200346870
CDS Mutation	c.214G>A
AA Mutation	p.Ala72Thr(p.A72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366834
Start	167156952:167156952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Trp(p.R294W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366834
Start	167157256:167157256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366834
Start	167157184:167157184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript