Colon Cancer: Gene >> AQP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58183987:58183987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740C>A
AA Mutation	p.Pro247His(p.P247H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58166713:58166713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751975709
CDS Mutation	c.152G>A
AA Mutation	p.Arg51Gln(p.R51Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58175017:58175017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146866709
CDS Mutation	c.476C>T
AA Mutation	p.Ala159Val(p.A159V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58166788:58166788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227G>A
AA Mutation	p.Gly76Asp(p.G76D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58138633:58138633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192641731
CDS Mutation	c.68C>T
AA Mutation	p.Ala23Val(p.A23V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58138656:58138656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91T>G
AA Mutation	p.Leu31Val(p.L31V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58179261:58179261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629A>G
AA Mutation	p.Asn210Ser(p.N210S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58166790:58166790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536480649
CDS Mutation	c.229G>A
AA Mutation	p.Gly77Ser(p.G77S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000219919
Start	58166712:58166712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370192849
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Ter(p.R51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AQP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58183975:58183975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.728T>C
AA Mutation	p.Phe243Ser(p.F243S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58173137:58173137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308C>T
AA Mutation	p.Pro103Leu(p.P103L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219919
Start	58138655:58138655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90C>A
AA Mutation	p.Phe30Leu(p.F30L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219919
Start	58175021:58175021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562183896
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219919
Start	58179208:58179208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript