Colon Cancer: Gene >> HLA-A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29942838:29942838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155T>C
AA Mutation	p.Val52Ala(p.V52A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29944284:29944284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772821446
CDS Mutation	c.782G>T
AA Mutation	p.Gly261Val(p.G261V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29943330:29943330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45542135
CDS Mutation	c.406G>A
AA Mutation	p.Gly136Arg(p.G136R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29944278:29944278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.776C>A
AA Mutation	p.Pro259His(p.P259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29944196:29944196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694T>C
AA Mutation	p.Phe232Leu(p.F232L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29944242:29944242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740A>G
AA Mutation	p.Asp247Gly(p.D247G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29943364:29943364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440A>G
AA Mutation	p.Tyr147Cys(p.Y147C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29943471:29943471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758168864
CDS Mutation	c.547T>C
AA Mutation	p.Tyr183His(p.Y183H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396634
Start	29943518:29943518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199474574
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396634
Start	29942569:29942569(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.19delC
AA Mutation	p.Arg7GlufsTer13(p.R7Efs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000396634
Start	29944395:29944395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893G>A
AA Mutation	p.Trp298Ter(p.W298*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000396634
Start	29942915:29942915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs281864736
CDS Mutation	c.232C>T
AA Mutation	p.Gln78Ter(p.Q78*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396634
Start	29942568:29942569(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.19dupC
AA Mutation	p.Arg7ProfsTer92(p.R7Pfs*92)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HLA-A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396634
Start	29944179:29944179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677G>A
AA Mutation	p.Arg226Lys(p.R226K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396634
Start	29944507:29944507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903T>G
Mutation Classification	Silent
Feature Type	Transcript