Colon Cancer: Gene >> CPEB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000507071
Start	15007398:15007398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>T
AA Mutation	p.Arg149Cys(p.R149C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000507071
Start	15007416:15007416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463G>A
AA Mutation	p.Gly155Arg(p.G155R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000507071
Start	15066370:15066370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533201180
CDS Mutation	c.1760G>A
AA Mutation	p.Arg587His(p.R587H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000507071
Start	15052446:15052446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898T>A
AA Mutation	p.Leu300Met(p.L300M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000507071
Start	15062123:15062123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405T>C
AA Mutation	p.Tyr469His(p.Y469H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507071
Start	15033192:15033192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507071
Start	15066206:15066206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1596C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000507071
Start	15066234:15066234(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1630delT
AA Mutation	p.Cys544ValfsTer31(p.C544Vfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000507071
Start	15066261:15066261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1651C>T
AA Mutation	p.Gln551Ter(p.Q551*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000507071
Start	15062174:15062174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456C>T
AA Mutation	p.Arg486Ter(p.R486*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000507071
Start	15033163:15033163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Ter(p.R273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000507071
Start	15052542:15052542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Ter(p.R332*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000507071
Start	15066233:15066234(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1630dupT
AA Mutation	p.Cys544LeufsTer12(p.C544Lfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000507071
Start	15059186:15059186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CPEB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000507071
Start	15066207:15066207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1597G>T
AA Mutation	p.Ala533Ser(p.A533S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000507071
Start	15058536:15058536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1242A>C
AA Mutation	p.Lys414Asn(p.K414N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000507071
Start	15066301:15066301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759238935
CDS Mutation	c.1691G>A
AA Mutation	p.Arg564His(p.R564H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript