Colon Cancer: Gene >> TAB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149378928:149378928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>A
AA Mutation	p.Ser338Tyr(p.S338Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149378248:149378248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333A>T
AA Mutation	p.Gln111His(p.Q111H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149379060:149379060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532837920
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149378661:149378661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746A>G
AA Mutation	p.Gln249Arg(p.Q249R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149378288:149378288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374508964
CDS Mutation	c.373G>A
AA Mutation	p.Glu125Lys(p.E125K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149378840:149378840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925C>A
AA Mutation	p.His309Asn(p.H309N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149379387:149379387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1472T>G
AA Mutation	p.Leu491Arg(p.L491R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149398047:149398047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1843C>A
AA Mutation	p.Leu615Ile(p.L615I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149409684:149409684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2047C>T
AA Mutation	p.Arg683Cys(p.R683C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149378542:149378542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.627G>T
AA Mutation	p.Gln209His(p.Q209H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367456
Start	149379319:149379319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138678250
CDS Mutation	c.1404C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367456
Start	149370032:149370032(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.38delT
AA Mutation	p.Leu13TyrfsTer48(p.L13Yfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000367456
Start	149397720:149397720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1720C>T
AA Mutation	p.Arg574Ter(p.R574*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TAB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149378526:149378526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611T>A
AA Mutation	p.Val204Glu(p.V204E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367456
Start	149370070:149370070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747627781
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript