Colon Cancer: Gene >> RASGRP3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000402538
Start	33555531:33555531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1543C>A
AA Mutation	p.Leu515Ile(p.L515I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000402538
Start	33519952:33519952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200007507
CDS Mutation	c.174G>A
AA Mutation	p.Met58Ile(p.M58I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33523913:33523913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551G>T
AA Mutation	p.Cys184Phe(p.C184F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33539113:33539113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370150483
CDS Mutation	c.1181C>T
AA Mutation	p.Thr394Met(p.T394M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000402538
Start	33520554:33520554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756271456
CDS Mutation	c.238T>C
AA Mutation	p.Tyr80His(p.Y80H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33549683:33549683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1474G>A
AA Mutation	p.Gly492Arg(p.G492R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33539110:33539110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746238359
CDS Mutation	c.1178C>T
AA Mutation	p.Thr393Met(p.T393M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33555559:33555559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571A>C
AA Mutation	p.Lys524Thr(p.K524T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33549740:33549740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1531T>C
AA Mutation	p.Cys511Arg(p.C511R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33516641:33516641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170G>T
AA Mutation	p.Cys57Phe(p.C57F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33558716:33558716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750A>G
AA Mutation	p.Arg584Gly(p.R584G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402538
Start	33527163:33527163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402538
Start	33519967:33519967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402538
Start	33534352:33534352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550267818
CDS Mutation	c.1113T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402538
Start	33527271:33527271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402538
Start	33524447:33524447(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.710delA
AA Mutation	p.Asn237IlefsTer5(p.N237Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000402538
Start	33515144:33515144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>A
AA Mutation	p.Ser3Ter(p.S3*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000402538
Start	33519956:33519956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178C>T
AA Mutation	p.Arg60Ter(p.R60*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RASGRP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33519957:33519957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369611073
CDS Mutation	c.179G>A
AA Mutation	p.Arg60Gln(p.R60Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33524481:33524481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740G>A
AA Mutation	p.Gly247Asp(p.G247D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33516563:33516563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92A>G
AA Mutation	p.Asn31Ser(p.N31S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33558277:33558277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375130686
CDS Mutation	c.1646G>A
AA Mutation	p.Arg549Gln(p.R549Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33519997:33519997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219G>T
AA Mutation	p.Lys73Asn(p.K73N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33521988:33521988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402G>T
AA Mutation	p.Gln134His(p.Q134H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000402538
Start	33516578:33516578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107G>T
AA Mutation	p.Arg36Ile(p.R36I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402538
Start	33539111:33539111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376346410
CDS Mutation	c.1179G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402538
Start	33549745:33549745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748035236
CDS Mutation	c.1536G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402538
Start	33516628:33516629(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.162dupA
AA Mutation	p.Leu55ThrfsTer15(p.L55Tfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript