Colon Cancer: Gene >> AQP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000199280
Start	49954684:49954684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772051028
CDS Mutation	c.580G>A
AA Mutation	p.Val194Ile(p.V194I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000199280
Start	49950970:49950970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>T
AA Mutation	p.Ala47Val(p.A47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000199280
Start	49954288:49954288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761436417
CDS Mutation	c.494G>T
AA Mutation	p.Gly165Val(p.G165V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000199280
Start	49950981:49950981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151G>T
AA Mutation	p.Gly51Cys(p.G51C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000199280
Start	49955466:49955466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674C>T
AA Mutation	p.Pro225Leu(p.P225L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000199280
Start	49955411:49955411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>A
AA Mutation	p.Gly207Arg(p.G207R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000199280
Start	49951169:49951169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144253988
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000199280
Start	49955425:49955425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AQP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000199280
Start	49950857:49950857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27C>A
AA Mutation	p.Phe9Leu(p.F9L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript