Colon Cancer: Gene >> RASGRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38512839:38512839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752166771
CDS Mutation	c.793C>T
AA Mutation	p.Arg265Cys(p.R265C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38494656:38494656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1985T>C
AA Mutation	p.Leu662Pro(p.L662P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38494659:38494659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1982C>A
AA Mutation	p.Ser661Tyr(p.S661Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38518296:38518296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517C>G
AA Mutation	p.Gln173Glu(p.Q173E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38511703:38511703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867G>T
AA Mutation	p.Gln289His(p.Q289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38507846:38507846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1122G>T
AA Mutation	p.Glu374Asp(p.E374D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38507767:38507767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201C>T
AA Mutation	p.Pro401Ser(p.P401S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310803
Start	38505885:38505885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310803
Start	38494625:38494625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2016C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310803
Start	38559825:38559825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310803
Start	38494538:38494538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2103T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000310803
Start	38498887:38498887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1780C>T
AA Mutation	p.Arg594Ter(p.R594*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RASGRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38501204:38501204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622C>T
AA Mutation	p.Pro541Leu(p.P541L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38498871:38498871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1796T>G
AA Mutation	p.Val599Gly(p.V599G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310803
Start	38511629:38511629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369326621
CDS Mutation	c.941C>T
AA Mutation	p.Ser314Leu(p.S314L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310803
Start	38507792:38507792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176A>G
Mutation Classification	Silent
Feature Type	Transcript