Colon Cancer: Gene >> ETV3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368192
Start	157125599:157125599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>T
AA Mutation	p.Val261Phe(p.V261F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368192
Start	157125377:157125377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003C>T
AA Mutation	p.His335Tyr(p.H335Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368192
Start	157124995:157124995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1385C>A
AA Mutation	p.Pro462His(p.P462H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368192
Start	157125431:157125431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Trp(p.R317W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368192
Start	157125817:157125817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563A>C
AA Mutation	p.Lys188Thr(p.K188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368192
Start	157135581:157135581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174G>T
AA Mutation	p.Gln58His(p.Q58H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368192
Start	157125957:157125957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368192
Start	157124949:157124949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368192
Start	157125384:157125384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368192
Start	157125711:157125711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368192
Start	157136324:157136324(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.29delA
AA Mutation	p.Lys10SerfsTer76(p.K10Sfs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ETV3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368192
Start	157134161:157134161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351C>A
AA Mutation	p.Phe117Leu(p.F117L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript