Colon Cancer: Gene >> NES

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672724:156672724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464A>T
AA Mutation	p.Arg488Ser(p.R488S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672903:156672903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751310959
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Trp(p.R429W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156669600:156669600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4588G>A
AA Mutation	p.Ala1530Thr(p.A1530T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672549:156672549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639A>G
AA Mutation	p.Lys547Glu(p.K547E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672167:156672167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2021A>T
AA Mutation	p.Asn674Ile(p.N674I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156671864:156671864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763450697
CDS Mutation	c.2324T>C
AA Mutation	p.Met775Thr(p.M775T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156669372:156669372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4816T>C
AA Mutation	p.Phe1606Leu(p.F1606L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672530:156672530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1658T>C
AA Mutation	p.Ile553Thr(p.I553T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672535:156672535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1653G>T
AA Mutation	p.Glu551Asp(p.E551D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156671606:156671606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2582A>G
AA Mutation	p.Asn861Ser(p.N861S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156670715:156670715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3473C>A
AA Mutation	p.Pro1158His(p.P1158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156670508:156670508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746890108
CDS Mutation	c.3680C>T
AA Mutation	p.Pro1227Leu(p.P1227L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156669667:156669667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4521G>T
AA Mutation	p.Leu1507Phe(p.L1507F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156670437:156670437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3751G>C
AA Mutation	p.Gly1251Arg(p.G1251R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156670343:156670343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3845G>A
AA Mutation	p.Ser1282Asn(p.S1282N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156671894:156671894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2294G>A
AA Mutation	p.Arg765Gln(p.R765Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672555:156672555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1633A>C
AA Mutation	p.Thr545Pro(p.T545P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156671360:156671360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2828C>A
AA Mutation	p.Pro943Gln(p.P943Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156671951:156671951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2237C>A
AA Mutation	p.Ser746Tyr(p.S746Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672202:156672202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1986G>T
AA Mutation	p.Glu662Asp(p.E662D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672344:156672344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1844A>C
AA Mutation	p.Lys615Thr(p.K615T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156669611:156669611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4577C>T
AA Mutation	p.Ala1526Val(p.A1526V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156671793:156671793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2395C>T
AA Mutation	p.Leu799Phe(p.L799F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368223
Start	156670678:156670678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368223
Start	156673485:156673485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749664076
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368223
Start	156671581:156671581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2607A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368223
Start	156672169:156672169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2019G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368223
Start	156676889:156676889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368223
Start	156672436:156672436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1752A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368223
Start	156670443:156670443(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3745delG
AA Mutation	p.Val1249CysfsTer11(p.V1249Cfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368223
Start	156673012:156673012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759081520
CDS Mutation	c.1176delC
AA Mutation	p.Thr393HisfsTer9(p.T393Hfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368223
Start	156671040:156671040(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3148delG
AA Mutation	p.Ala1050ProfsTer14(p.A1050Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368223
Start	156669533:156669533(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4655delG
AA Mutation	p.Gly1552GlufsTer2(p.G1552Efs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368223
Start	156669874:156669874(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4314delG
AA Mutation	p.Pro1439GlnfsTer11(p.P1439Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NES

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156675289:156675289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835G>A
AA Mutation	p.Ala279Thr(p.A279T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156670722:156670722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529267878
CDS Mutation	c.3466G>A
AA Mutation	p.Glu1156Lys(p.E1156K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368223
Start	156672280:156672280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1908G>T
AA Mutation	p.Met636Ile(p.M636I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368223
Start	156670630:156670630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149557132
CDS Mutation	c.3558G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368223
Start	156677057:156677057(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.208delC
AA Mutation	p.Arg70AlafsTer40(p.R70Afs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000368223
Start	156672558:156672558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1630G>T
AA Mutation	p.Glu544Ter(p.E544*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript