Colon Cancer: Gene >> TUBB4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340384
Start	137242589:137242589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371C>T
AA Mutation	p.Ala124Val(p.A124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340384
Start	137243074:137243074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Val286Met(p.V286M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340384
Start	137242657:137242657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439A>G
AA Mutation	p.Met147Val(p.M147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340384
Start	137242602:137242602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340384
Start	137243445:137243445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770443576
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000340384
Start	137241382:137241382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22C>T
AA Mutation	p.Gln8Ter(p.Q8*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TUBB4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340384
Start	137243436:137243436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218G>T
AA Mutation	p.Met406Ile(p.M406I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340384
Start	137241387:137241387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript