Colon Cancer: Gene >> TRO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54923364:54923364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832C>G
AA Mutation	p.Leu278Val(p.L278V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54928682:54928682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1958C>A
AA Mutation	p.Ala653Asp(p.A653D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54927088:54927088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1746C>A
AA Mutation	p.Asp582Glu(p.D582E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54928916:54928916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2192C>T
AA Mutation	p.Ala731Val(p.A731V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54930953:54930953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752478190
CDS Mutation	c.4229C>T
AA Mutation	p.Pro1410Leu(p.P1410L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54923238:54923238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706G>T
AA Mutation	p.Gly236Cys(p.G236C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54929698:54929698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2974G>A
AA Mutation	p.Ala992Thr(p.A992T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54930497:54930497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3773G>C
AA Mutation	p.Gly1258Ala(p.G1258A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54923602:54923602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070C>T
AA Mutation	p.Thr357Ile(p.T357I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54929941:54929941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757678937
CDS Mutation	c.3217G>A
AA Mutation	p.Val1073Ile(p.V1073I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54922932:54922932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>A
AA Mutation	p.Ala134Thr(p.A134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54924511:54924511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200113081
CDS Mutation	c.1297C>T
AA Mutation	p.Arg433Trp(p.R433W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54930446:54930446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3722G>T
AA Mutation	p.Gly1241Val(p.G1241V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54929480:54929480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2756T>C
AA Mutation	p.Phe919Ser(p.F919S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54926481:54926481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1649C>G
AA Mutation	p.Ala550Gly(p.A550G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54929659:54929659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2935T>G
AA Mutation	p.Phe979Val(p.F979V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54927718:54927718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1815C>A
AA Mutation	p.Phe605Leu(p.F605L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54929366:54929366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2642G>C
AA Mutation	p.Ser881Thr(p.S881T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54925678:54925678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1572G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54930228:54930228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54930504:54930504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3780T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54924694:54924694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1366T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54928644:54928644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756724040
CDS Mutation	c.1920C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54923006:54923006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54930762:54930762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54930051:54930051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs74903554
CDS Mutation	c.3327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000173898
Start	54929826:54929826(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3102delC
AA Mutation	p.Ser1034ArgfsTer10(p.S1034Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000173898
Start	54925613:54925613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507G>T
AA Mutation	p.Glu503Ter(p.E503*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54926619:54926619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201094980
CDS Mutation	c.1694G>A
AA Mutation	p.Arg565His(p.R565H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54927732:54927732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1829G>A
AA Mutation	p.Arg610His(p.R610H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54930350:54930350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3626T>C
AA Mutation	p.Phe1209Ser(p.F1209S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000173898
Start	54929369:54929369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770587637
CDS Mutation	c.2645C>T
AA Mutation	p.Ala882Val(p.A882V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173898
Start	54930621:54930621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201030396
CDS Mutation	c.3897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000173898
Start	54930838:54930839(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4116_4126dupCACTGGTGTTG
AA Mutation	p.Gly1376AlafsTer79(p.G1376Afs*79)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript