Colon Cancer: Gene >> AVPR1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206116056:206116056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835A>T
AA Mutation	p.Thr279Ser(p.T279S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206116026:206116026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>A
AA Mutation	p.Ala289Thr(p.A289T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206110413:206110413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051C>T
AA Mutation	p.Arg351Cys(p.R351C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206116581:206116581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Asp104Asn(p.D104N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206116806:206116806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Trp(p.R29W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206116058:206116058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833G>A
AA Mutation	p.Arg278Gln(p.R278Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206116301:206116301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590G>A
AA Mutation	p.Arg197Gln(p.R197Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206116679:206116679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212T>G
AA Mutation	p.Leu71Arg(p.L71R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367126
Start	206116267:206116267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367126
Start	206116473:206116473(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.418delC
AA Mutation	p.Leu140CysfsTer38(p.L140Cfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AVPR1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206110505:206110505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959T>C
AA Mutation	p.Phe320Ser(p.F320S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206116022:206116022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869A>G
AA Mutation	p.Tyr290Cys(p.Y290C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367126
Start	206115980:206115980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.911C>A
AA Mutation	p.Ser304Tyr(p.S304Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367126
Start	206116042:206116042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849C>A
Mutation Classification	Silent
Feature Type	Transcript