Colon Cancer: Gene >> HLA-B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355582:31355582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630G>T
AA Mutation	p.Lys210Asn(p.K210N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31356944:31356944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87G>A
AA Mutation	p.Met29Ile(p.M29I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31356883:31356883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148G>T
AA Mutation	p.Gly50Cys(p.G50C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355430:31355430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782G>C
AA Mutation	p.Gly261Ala(p.G261A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000412585
Start	31355156:31355156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41555623
CDS Mutation	c.963G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31357140:31357140(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.19delC
AA Mutation	p.Arg7GlufsTer13(p.R7Efs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31355586:31355586(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.626delC
AA Mutation	p.Pro209GlnfsTer5(p.P209Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31356791:31356791(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.240delG
AA Mutation	p.Pro81ArgfsTer70(p.P81Rfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31355569:31355569(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.643delC
AA Mutation	p.His215ThrfsTer11(p.H215Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31355202:31355202(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.917delT
AA Mutation	p.Val306AlafsTer13(p.V306Afs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31356818:31356818(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.213delG
AA Mutation	p.Arg72GlyfsTer5(p.R72Gfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000412585
Start	31355488:31355488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41564218
CDS Mutation	c.724C>T
AA Mutation	p.Gln242Ter(p.Q242*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000412585
Start	31356779:31356779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137854679
CDS Mutation	c.252G>A
AA Mutation	p.Trp84Ter(p.W84*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31356416:31356417(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.369_370insT
AA Mutation	p.Gly124TrpfsTer15(p.G124Wfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31355185:31355186(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.933dupT
AA Mutation	p.Val312CysfsTer22(p.V312Cfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000412585
Start	31356687:31356687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000412585
Start	31355224:31355224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000412585
Start	31355105:31355105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HLA-B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31357140:31357140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19C>G
AA Mutation	p.Arg7Gly(p.R7G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript