Colon Cancer: Gene >> VAV1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6829883:6829883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1363C>T
AA Mutation	p.Arg455Trp(p.R455W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6852988:6852988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2241G>T
AA Mutation	p.Gln747His(p.Q747H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6772995:6772995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771269172
CDS Mutation	c.188G>A
AA Mutation	p.Arg63His(p.R63H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6848018:6848018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2033G>A
AA Mutation	p.Arg678Gln(p.R678Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6772847:6772847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40T>C
AA Mutation	p.Cys14Arg(p.C14R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6822282:6822282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>A
AA Mutation	p.Asp171Asn(p.D171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6833920:6833920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744C>T
AA Mutation	p.Arg582Cys(p.R582C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6826644:6826644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860T>C
AA Mutation	p.Val287Ala(p.V287A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6828637:6828637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108G>A
AA Mutation	p.Val370Met(p.V370M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6821661:6821661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>A
AA Mutation	p.Ala121Thr(p.A121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6828435:6828435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040C>T
AA Mutation	p.Thr347Met(p.T347M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6820759:6820759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262C>T
AA Mutation	p.Leu88Phe(p.L88F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6836467:6836467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754314420
CDS Mutation	c.1813G>A
AA Mutation	p.Gly605Arg(p.G605R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6836508:6836508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1854G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6822281:6822281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150109367
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6828853:6828853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6836538:6836538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771559881
CDS Mutation	c.1884G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6833217:6833217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199798227
CDS Mutation	c.1542C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6822275:6822275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201079372
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6822311:6822311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771609375
CDS Mutation	c.540G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VAV1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6828866:6828866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231A>T
AA Mutation	p.Ile411Phe(p.I411F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6829835:6829835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1315G>T
AA Mutation	p.Asp439Tyr(p.D439Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6853965:6853965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2351T>G
AA Mutation	p.Phe784Cys(p.F784C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6857070:6857070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2501C>A
AA Mutation	p.Ala834Asp(p.A834D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6821828:6821828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>T
AA Mutation	p.Asp140Tyr(p.D140Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6832111:6832111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1419G>A
Mutation Classification	Silent
Feature Type	Transcript