Colon Cancer: Gene >> ETS1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000319397
Start	128489292:128489292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401A>C
AA Mutation	p.Lys134Thr(p.K134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319397
Start	128484906:128484906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647C>T
AA Mutation	p.Thr216Ile(p.T216I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319397
Start	128486115:128486115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319397
Start	128484836:128484836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319397
Start	128462394:128462394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319397
Start	128480252:128480252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000319397
Start	128480408:128480408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>G
AA Mutation	p.Tyr258Ter(p.Y258*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319397
Start	128484945:128484946(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.607_608insGAAGAAAT
AA Mutation	p.Asn203ArgfsTer56(p.N203Rfs*56)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ETS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319397
Start	128462396:128462396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774575276
CDS Mutation	c.1291G>A
AA Mutation	p.Ala431Thr(p.A431T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319397
Start	128480346:128480346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.836G>T
AA Mutation	p.Arg279Leu(p.R279L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319397
Start	128484853:128484853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>T
AA Mutation	p.Asp234Tyr(p.D234Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319397
Start	128489335:128489335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358T>A
AA Mutation	p.Phe120Ile(p.F120I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319397
Start	128521938:128521938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000319397
Start	128490532:128490532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>T
AA Mutation	p.Glu43Ter(p.E43*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript