Colon Cancer: Gene >> VIPR2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262178
Start	159058578:159058578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358A>G
AA Mutation	p.Ile120Val(p.I120V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159031854:159031854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1117G>A
AA Mutation	p.Val373Ile(p.V373I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159103827:159103827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287A>G
AA Mutation	p.Asp96Gly(p.D96G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159103764:159103764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350A>C
AA Mutation	p.Glu117Ala(p.E117A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159043165:159043165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467G>A
AA Mutation	p.Cys156Tyr(p.C156Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159034294:159034294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890T>C
AA Mutation	p.Val297Ala(p.V297A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159109884:159109884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750654613
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Trp(p.R63W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159035972:159035972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765248907
CDS Mutation	c.789G>C
AA Mutation	p.Arg263Ser(p.R263S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262178
Start	159103796:159103796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763829150
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262178
Start	159142453:159142453(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.144delA
AA Mutation	p.Lys48AsnfsTer42(p.K48Nfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000262178
Start	159030771:159030771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1162C>T
AA Mutation	p.Arg388Ter(p.R388*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> VIPR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159032003:159032003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747989359
CDS Mutation	c.1036G>A
AA Mutation	p.Val346Met(p.V346M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262178
Start	159058564:159058564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372T>G
AA Mutation	p.Ile124Met(p.I124M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262178
Start	159043110:159043110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522C>A
Mutation Classification	Silent
Feature Type	Transcript