Colon Cancer: Gene >> VCL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74083506:74083506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759961842
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Cys(p.R339C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74103835:74103835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759356162
CDS Mutation	c.2038C>T
AA Mutation	p.Arg680Cys(p.R680C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74074796:74074796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146910007
CDS Mutation	c.676G>A
AA Mutation	p.Ala226Thr(p.A226T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74112069:74112069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534101808
CDS Mutation	c.2906C>T
AA Mutation	p.Ala969Val(p.A969V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74112015:74112015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368570586
CDS Mutation	c.2852C>G
AA Mutation	p.Pro951Arg(p.P951R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74105347:74105347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751458490
CDS Mutation	c.2428G>A
AA Mutation	p.Asp810Asn(p.D810N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74111981:74111981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2818C>A
AA Mutation	p.Pro940Thr(p.P940T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74070978:74070978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Cys(p.R132C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74074809:74074809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749628307
CDS Mutation	c.689G>A
AA Mutation	p.Arg230His(p.R230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000211998
Start	74109155:74109155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2744A>G
AA Mutation	p.Lys915Arg(p.K915R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000211998
Start	74112004:74112004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566296495
CDS Mutation	c.2841C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000211998
Start	73998298:73998298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91G>T
AA Mutation	p.Glu31Ter(p.E31*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000211998
Start	74090028:74090028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>A
AA Mutation	p.Trp394Ter(p.W394*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000211998
Start	74071084:74071084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.499+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> VCL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000211998
Start	74118114:74118114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3350G>A
AA Mutation	p.Arg1117Gln(p.R1117Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript