Colon Cancer: Gene >> ETS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38819516:38819516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825C>A
AA Mutation	p.Asp275Glu(p.D275E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38810055:38810055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21G>T
AA Mutation	p.Lys7Asn(p.K7N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38818456:38818456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621G>A
AA Mutation	p.Met207Ile(p.M207I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38817080:38817080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578G>A
AA Mutation	p.Ser193Asn(p.S193N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38814907:38814907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431A>C
AA Mutation	p.Lys144Thr(p.K144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38822680:38822680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201C>T
AA Mutation	p.Arg401Cys(p.R401C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38821699:38821699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189G>A
AA Mutation	p.Asp397Asn(p.D397N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360214
Start	38822838:38822838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1359G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ETS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38821654:38821654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1144A>G
AA Mutation	p.Ile382Val(p.I382V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38819697:38819697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1006C>G
AA Mutation	p.Gln336Glu(p.Q336E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360214
Start	38819698:38819698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007A>T
AA Mutation	p.Gln336Leu(p.Q336L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript