Colon Cancer: Gene >> TAB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216160
Start	39419584:39419584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746857619
CDS Mutation	c.730G>A
AA Mutation	p.Gly244Arg(p.G244R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216160
Start	39415639:39415639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779843526
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Cys(p.R104C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216160
Start	39417804:39417804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748314614
CDS Mutation	c.505G>A
AA Mutation	p.Val169Ile(p.V169I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216160
Start	39417792:39417792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493G>T
AA Mutation	p.Gly165Trp(p.G165W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216160
Start	39426768:39426768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138903748
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216160
Start	39428168:39428168(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1296delC
AA Mutation	p.Thr433ProfsTer9(p.T433Pfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TAB1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216160
Start	39430219:39430219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375542675
CDS Mutation	c.1512G>A
Mutation Classification	Silent
Feature Type	Transcript