Colon Cancer: Gene >> CBFA2T3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88879432:88879432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1500G>T
AA Mutation	p.Gln500His(p.Q500H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88892266:88892266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758562596
CDS Mutation	c.599G>A
AA Mutation	p.Arg200His(p.R200H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88881384:88881384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1309C>G
AA Mutation	p.Arg437Gly(p.R437G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88892329:88892329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.536G>A
AA Mutation	p.Arg179His(p.R179H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88885090:88885090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760610315
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358His(p.R358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88892438:88892438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427T>C
AA Mutation	p.Cys143Arg(p.C143R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88886099:88886099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88976662:88976662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146G>A
AA Mutation	p.Gly49Asp(p.G49D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88892350:88892350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370027238
CDS Mutation	c.515G>A
AA Mutation	p.Arg172Gln(p.R172Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88879403:88879403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535005481
CDS Mutation	c.1529C>T
AA Mutation	p.Ser510Leu(p.S510L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000268679
Start	88880786:88880786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405G>A
AA Mutation	p.Val469Met(p.V469M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268679
Start	88881310:88881310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1383T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268679
Start	88898142:88898142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268679
Start	88885134:88885134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268679
Start	88877159:88877159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1779C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CBFA2T3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88879392:88879392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760316068
CDS Mutation	c.1540C>T
AA Mutation	p.Arg514Cys(p.R514C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268679
Start	88885090:88885090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760610315
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358His(p.R358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript