Colon Cancer: Gene >> VAV2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133787256:133787256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1412A>G
AA Mutation	p.His471Arg(p.H471R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133784324:133784324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1627T>A
AA Mutation	p.Phe543Ile(p.F543I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133939197:133939197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227G>A
AA Mutation	p.Arg76His(p.R76H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133768570:133768570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2461G>T
AA Mutation	p.Ala821Ser(p.A821S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133812130:133812130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.536A>C
AA Mutation	p.Glu179Ala(p.E179A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133770447:133770447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2278G>A
AA Mutation	p.Asp760Asn(p.D760N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133774971:133774971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2099G>A
AA Mutation	p.Arg700Gln(p.R700Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133776077:133776077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1969C>T
AA Mutation	p.Pro657Ser(p.P657S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133785858:133785858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1450C>A
AA Mutation	p.Leu484Ile(p.L484I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371850
Start	133768448:133768448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747438873
CDS Mutation	c.2583C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371850
Start	133775000:133775000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs7875953
CDS Mutation	c.2070C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371850
Start	133797791:133797791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.855G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371850
Start	133768508:133768508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764709519
CDS Mutation	c.2523C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VAV2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133777410:133777410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1944G>T
AA Mutation	p.Lys648Asn(p.K648N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133768524:133768524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771858287
CDS Mutation	c.2507C>T
AA Mutation	p.Ser836Leu(p.S836L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371850
Start	133939116:133939116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766660632
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371850
Start	133771971:133771971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543238251
CDS Mutation	c.2211C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371850
Start	133772022:133772022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2160C>T
Mutation Classification	Silent
Feature Type	Transcript