Colon Cancer: Gene >> RABGEF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66808955:66808955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777685946
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Cys(p.R397C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66808943:66808943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1177G>A
AA Mutation	p.Glu393Lys(p.E393K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66809054:66809054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288C>A
AA Mutation	p.Leu430Ile(p.L430I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66808919:66808919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757460921
CDS Mutation	c.1153G>A
AA Mutation	p.Ala385Thr(p.A385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66809175:66809175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760257544
CDS Mutation	c.1409A>G
AA Mutation	p.Tyr470Cys(p.Y470C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66805338:66805338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756436887
CDS Mutation	c.1061G>A
AA Mutation	p.Arg354His(p.R354H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66809085:66809085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1319G>T
AA Mutation	p.Arg440Met(p.R440M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66805335:66805335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767995746
CDS Mutation	c.1058C>T
AA Mutation	p.Thr353Met(p.T353M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66775334:66775334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329G>A
AA Mutation	p.Arg110His(p.R110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380828
Start	66808942:66808942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380828
Start	66805336:66805336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753077071
CDS Mutation	c.1059G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RABGEF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380828
Start	66783718:66783718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432A>C
AA Mutation	p.Gln144His(p.Q144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380828
Start	66775380:66775380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756497032
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000380828
Start	66808991:66808991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225G>T
AA Mutation	p.Glu409Ter(p.E409*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript