Colon Cancer: Gene >> TUBB4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6496015:6496015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6495594:6495594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905C>T
AA Mutation	p.Ala302Val(p.A302V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6496138:6496138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Trp(p.R121W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6495748:6495748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Cys(p.R251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6495330:6495330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1169G>A
AA Mutation	p.Arg390Gln(p.R390Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6495771:6495771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.728C>T
AA Mutation	p.Pro243Leu(p.P243L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6495751:6495751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748C>A
AA Mutation	p.Leu250Met(p.L250M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6495946:6495946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Ala185Thr(p.A185T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264071
Start	6495404:6495404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148507956
CDS Mutation	c.1095G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264071
Start	6495518:6495518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780784525
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264071
Start	6495266:6495266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138128036
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264071
Start	6496169:6496169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770749775
CDS Mutation	c.330A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264071
Start	6501525:6501525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375230837
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264071
Start	6495617:6495617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755875935
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264071
Start	6495437:6495437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748787734
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264071
Start	6496077:6496077(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.422delG
AA Mutation	p.Gly141ValfsTer24(p.G141Vfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TUBB4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264071
Start	6495447:6495447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052C>T
AA Mutation	p.Thr351Met(p.T351M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript