Colon Cancer: Gene >> BCAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24849794:24849794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666G>T
AA Mutation	p.Lys222Asn(p.K222N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24842111:24842111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788T>G
AA Mutation	p.Leu263Arg(p.L263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24829852:24829852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749915074
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Cys(p.R364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24832824:24832824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943G>A
AA Mutation	p.Asp315Asn(p.D315N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24901833:24901833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59A>C
AA Mutation	p.Glu20Ala(p.E20A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24849920:24849920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540A>C
AA Mutation	p.Lys180Asn(p.K180N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24849939:24849939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521G>A
AA Mutation	p.Gly174Glu(p.G174E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24894465:24894465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89T>C
AA Mutation	p.Leu30Pro(p.L30P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24842105:24842105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794T>C
AA Mutation	p.Leu265Pro(p.L265P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261192
Start	24894335:24894335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000261192
Start	24881387:24881387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754324341
CDS Mutation	c.304C>T
AA Mutation	p.Arg102Ter(p.R102*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000261192
Start	24881398:24881398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293T>A
AA Mutation	p.Leu98Ter(p.L98*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BCAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261192
Start	24881326:24881326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365G>A
AA Mutation	p.Arg122His(p.R122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261192
Start	24878649:24878649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Val131Ile(p.V131I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000261192
Start	24818040:24818040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>T
AA Mutation	p.Glu377Ter(p.E377*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript