Colon Cancer: Gene >> OPCML

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132420240:132420240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991C>A
AA Mutation	p.Leu331Ile(p.L331I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657159:132657159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>A
AA Mutation	p.Glu110Lys(p.E110K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132942956:132942956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749718972
CDS Mutation	c.137C>T
AA Mutation	p.Thr46Met(p.T46M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132942936:132942936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Ala53Thr(p.A53T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132943088:132943088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5G>C
AA Mutation	p.Gly2Ala(p.G2A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657276:132657276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770223558
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Cys(p.R71C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331898
Start	132529062:132529062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525G>T
AA Mutation	p.Lys175Asn(p.K175N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657269:132657269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>A
AA Mutation	p.Thr73Asn(p.T73N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132529127:132529127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460A>T
AA Mutation	p.Thr154Ser(p.T154S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132942999:132942999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>T
AA Mutation	p.Arg32Cys(p.R32C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132529155:132529155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432C>A
AA Mutation	p.Asp144Glu(p.D144E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132943065:132943065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28C>T
AA Mutation	p.Pro10Ser(p.P10S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132437268:132437268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618C>A
AA Mutation	p.Asn206Lys(p.N206K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132436096:132436096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132436234:132436234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132436670:132436670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132437253:132437253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780275496
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331898
Start	132420241:132420242(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.989_990delGT
AA Mutation	p.Cys330SerfsTer73(p.C330Sfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331898
Start	132437233:132437234(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.652dupA
AA Mutation	p.Ile218AsnfsTer28(p.I218Nfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> OPCML

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657227:132657227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260G>A
AA Mutation	p.Arg87His(p.R87H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657161:132657161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326A>C
AA Mutation	p.Asp109Ala(p.D109A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132437285:132437285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148167692
CDS Mutation	c.601G>A
AA Mutation	p.Glu201Lys(p.E201K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132436123:132436123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747062268
CDS Mutation	c.900C>A
AA Mutation	p.Asn300Lys(p.N300K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657157:132657157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330A>C
AA Mutation	p.Glu110Asp(p.E110D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132436211:132436211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812G>T
AA Mutation	p.Arg271Met(p.R271M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132437256:132437256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747460633
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132657151:132657151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369569350
CDS Mutation	c.336G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132420244:132420244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132437271:132437271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780936478
CDS Mutation	c.615G>A
Mutation Classification	Silent
Feature Type	Transcript