Colon Cancer: Gene >> VANGL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160419339:160419339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530G>A
AA Mutation	p.Arg177His(p.R177H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160419417:160419417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766519016
CDS Mutation	c.608G>A
AA Mutation	p.Arg203His(p.R203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160416069:160416069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754493544
CDS Mutation	c.79C>T
AA Mutation	p.Arg27Trp(p.R27W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160419104:160419104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295G>A
AA Mutation	p.Val99Ile(p.V99I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160419471:160419471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662C>T
AA Mutation	p.Ser221Leu(p.S221L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160425139:160425139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552247057
CDS Mutation	c.1327G>A
AA Mutation	p.Ala443Thr(p.A443T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160419437:160419437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Cys(p.R210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160419564:160419564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160419353:160419353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Cys(p.R182C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160421171:160421171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267607167
CDS Mutation	c.1057C>T
AA Mutation	p.Arg353Cys(p.R353C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368061
Start	160419571:160419571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139084368
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368061
Start	160424265:160424265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1287G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368061
Start	160419166:160419166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000368061
Start	160420415:160420415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805C>T
AA Mutation	p.Gln269Ter(p.Q269*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000368061
Start	160420410:160420410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> VANGL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368061
Start	160415896:160415896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59C>T
AA Mutation	p.Ser20Phe(p.S20F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript