Colon Cancer: Gene >> TAZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000601016
Start	154414118:154414118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388G>A
AA Mutation	p.Ala130Thr(p.A130T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000601016
Start	154420924:154420924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799A>G
AA Mutation	p.Thr267Ala(p.T267A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000601016
Start	154420731:154420731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773C>T
AA Mutation	p.Ser258Leu(p.S258L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000601016
Start	154413513:154413513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316A>G
AA Mutation	p.Lys106Glu(p.K106E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000601016
Start	154420222:154420222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140751478
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000601016
Start	154420705:154420705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TAZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000601016
Start	154419725:154419725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375663114
CDS Mutation	c.562G>A
AA Mutation	p.Glu188Lys(p.E188K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript