Colon Cancer: Gene >> VIL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218449241:218449241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2389G>T
AA Mutation	p.Asp797Tyr(p.D797Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218440812:218440812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2320A>T
AA Mutation	p.Asn774Tyr(p.N774Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218432800:218432800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1349A>C
AA Mutation	p.Gln450Pro(p.Q450P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218430749:218430749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973C>A
AA Mutation	p.Pro325Thr(p.P325T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218425771:218425771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746568854
CDS Mutation	c.307G>A
AA Mutation	p.Glu103Lys(p.E103K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218423794:218423794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146567646
CDS Mutation	c.16G>A
AA Mutation	p.Ala6Thr(p.A6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218437176:218437176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2024C>A
AA Mutation	p.Ala675Glu(p.A675E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248444
Start	218428058:218428058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199702756
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248444
Start	218429944:218429944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368273701
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VIL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218423794:218423794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146567646
CDS Mutation	c.16G>A
AA Mutation	p.Ala6Thr(p.A6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218432053:218432053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369865042
CDS Mutation	c.1211G>A
AA Mutation	p.Arg404His(p.R404H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248444
Start	218449315:218449315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2463G>T
AA Mutation	p.Lys821Asn(p.K821N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript