Colon Cancer: Gene >> TUBB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317702
Start	12325519:12325519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>T
AA Mutation	p.Gly244Cys(p.G244C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317702
Start	12325540:12325540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756545880
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Cys(p.R251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317702
Start	12325724:12325724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935C>T
AA Mutation	p.Thr312Ile(p.T312I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317702
Start	12325207:12325207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418G>C
AA Mutation	p.Gly140Arg(p.G140R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317702
Start	12325879:12325879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090G>A
AA Mutation	p.Ala364Thr(p.A364T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317702
Start	12325563:12325563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317702
Start	12325602:12325602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575654137
CDS Mutation	c.813G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317702
Start	12325770:12325770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758456776
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317702
Start	12325116:12325116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TUBB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317702
Start	12325983:12325983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1194C>A
AA Mutation	p.Phe398Leu(p.F398L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317702
Start	12326121:12326121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376872570
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript