Colon Cancer: Gene >> AQP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383168
Start	26862321:26862321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308C>T
AA Mutation	p.Ala103Val(p.A103V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383168
Start	26856382:26856382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801C>A
AA Mutation	p.Ser267Arg(p.S267R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383168
Start	26865685:26865685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5G>C
AA Mutation	p.Ser2Thr(p.S2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383168
Start	26862288:26862288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.341A>C
AA Mutation	p.Lys114Thr(p.K114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000383168
Start	26861291:26861291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452A>T
AA Mutation	p.His151Leu(p.H151L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383168
Start	26860796:26860796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000383168
Start	26860783:26860783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>T
AA Mutation	p.Glu228Ter(p.E228*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AQP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383168
Start	26856243:26856243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.940G>T
AA Mutation	p.Asp314Tyr(p.D314Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript