Colon Cancer: Gene >> ETV1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13906555:13906555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985T>C
AA Mutation	p.Tyr329His(p.Y329H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13931667:13931667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772105404
CDS Mutation	c.637C>T
AA Mutation	p.Arg213Cys(p.R213C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13931744:13931744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779937870
CDS Mutation	c.560G>A
AA Mutation	p.Arg187His(p.R187H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13931745:13931745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748346103
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Cys(p.R187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13906591:13906591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949A>G
AA Mutation	p.Lys317Glu(p.K317E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13931738:13931738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566A>T
AA Mutation	p.Gln189Leu(p.Q189L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13900793:13900793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1157A>G
AA Mutation	p.Tyr386Cys(p.Y386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13900802:13900802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148C>T
AA Mutation	p.Ala383Val(p.A383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13931681:13931681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623G>A
AA Mutation	p.Arg208His(p.R208H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13909635:13909635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937G>A
AA Mutation	p.Asp313Asn(p.D313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13939241:13939241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241T>G
AA Mutation	p.Phe81Val(p.F81V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13895928:13895928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372G>A
AA Mutation	p.Ala458Thr(p.A458T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405218
Start	13935851:13935851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405218
Start	13939212:13939212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405218
Start	13939122:13939122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405218
Start	13931608:13931608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000405218
Start	13935848:13935848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.414delC
AA Mutation	p.Thr139HisfsTer116(p.T139Hfs*116)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000405218
Start	13906546:13906546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Ter(p.R332*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ETV1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13988160:13988160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59G>T
AA Mutation	p.Arg20Ile(p.R20I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000405218
Start	13931745:13931745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748346103
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Cys(p.R187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405218
Start	13900756:13900756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript