Colon Cancer: Gene >> CTAGE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22416709:22416709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103G>T
AA Mutation	p.Arg368Met(p.R368M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22415758:22415758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2054G>A
AA Mutation	p.Gly685Glu(p.G685E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22416130:22416130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1682C>T
AA Mutation	p.Ala561Val(p.A561V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22417654:22417654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158C>A
AA Mutation	p.Ser53Tyr(p.S53Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22417477:22417477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335T>C
AA Mutation	p.Val112Ala(p.V112A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22415668:22415668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2144C>T
AA Mutation	p.Ala715Val(p.A715V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22417802:22417802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10G>A
AA Mutation	p.Asp4Asn(p.D4N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22416851:22416851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961A>G
AA Mutation	p.Thr321Ala(p.T321A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391403
Start	22415748:22415748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777199287
CDS Mutation	c.2064C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391403
Start	22417449:22417449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391403
Start	22416920:22416920(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.892delA
AA Mutation	p.Thr298ProfsTer2(p.T298Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391403
Start	22415590:22415590(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs777304069
CDS Mutation	c.2222delC
AA Mutation	p.Pro741GlnfsTer15(p.P741Qfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391403
Start	22415596:22415596(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs770098578
CDS Mutation	c.2216delT
AA Mutation	p.Phe739SerfsTer17(p.F739Sfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391403
Start	22416498:22416499(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1313_1314insCAAA
AA Mutation	p.Ala439LysfsTer3(p.A439Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CTAGE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22417615:22417615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197T>G
AA Mutation	p.Phe66Cys(p.F66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391403
Start	22415867:22415867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1945C>A
AA Mutation	p.Leu649Ile(p.L649I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript