Colon Cancer: Gene >> ETV6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11869510:11869510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550T>A
AA Mutation	p.Ser184Thr(p.S184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11884558:11884558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123G>A
AA Mutation	p.Gly375Arg(p.G375R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11884577:11884577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142G>A
AA Mutation	p.Gly381Glu(p.G381E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11884540:11884540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Trp(p.R369W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11869601:11869601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs724159947
CDS Mutation	c.641C>T
AA Mutation	p.Pro214Leu(p.P214L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11884575:11884575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1140G>T
AA Mutation	p.Trp380Cys(p.W380C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11839248:11839248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272G>A
AA Mutation	p.Gly91Asp(p.G91D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11885959:11885959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186A>G
AA Mutation	p.Arg396Gly(p.R396G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396373
Start	11752572:11752572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762064732
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396373
Start	11869941:11869941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374744954
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396373
Start	11884542:11884542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396373
Start	11839228:11839228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396373
Start	11752551:11752552(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.136_137delGA
AA Mutation	p.Asp46LeufsTer19(p.D46Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396373
Start	11853512:11853513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.416_417delCT
AA Mutation	p.Ser139TyrfsTer14(p.S139Yfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000396373
Start	11869633:11869633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673C>T
AA Mutation	p.Gln225Ter(p.Q225*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396373
Start	11853483:11853484(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.391dupT
AA Mutation	p.Ser131PhefsTer23(p.S131Ffs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ETV6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11869813:11869813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376242225
CDS Mutation	c.853G>A
AA Mutation	p.Val285Met(p.V285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11885930:11885930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1157G>T
AA Mutation	p.Arg386Ile(p.R386I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript