Colon Cancer: Gene >> TUBG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251412
Start	42663009:42663009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436G>A
AA Mutation	p.Gly146Ser(p.G146S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251412
Start	42666670:42666670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409His(p.R409H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251412
Start	42666660:42666660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372512326
CDS Mutation	c.1216G>A
AA Mutation	p.Glu406Lys(p.E406K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000251412
Start	42666386:42666386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574597874
CDS Mutation	c.1060G>A
AA Mutation	p.Ala354Thr(p.A354T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000251412
Start	42662979:42662979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753214599
CDS Mutation	c.406G>A
AA Mutation	p.Val136Met(p.V136M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251412
Start	42665701:42665701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251412
Start	42665511:42665511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251412
Start	42665719:42665719(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780176927
CDS Mutation	c.738delC
AA Mutation	p.Gly247AlafsTer3(p.G247Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000251412
Start	42663039:42663039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768619979
CDS Mutation	c.466C>T
AA Mutation	p.Arg156Ter(p.R156*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TUBG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251412
Start	42666129:42666129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.886C>T
AA Mutation	p.Arg296Trp(p.R296W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000251412
Start	42659884:42659884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>T
AA Mutation	p.Glu34Ter(p.E34*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript