Colon Cancer: Gene >> CPEB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173890782:173890782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049G>A
AA Mutation	p.Arg350His(p.R350H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173951933:173951933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752472463
CDS Mutation	c.1775G>A
AA Mutation	p.Arg592Gln(p.R592Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173890695:173890695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962T>C
AA Mutation	p.Leu321Pro(p.L321P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173890217:173890217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484G>A
AA Mutation	p.Ala162Thr(p.A162T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173951924:173951924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1766G>A
AA Mutation	p.Arg589Gln(p.R589Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173910541:173910541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148567441
CDS Mutation	c.1144G>A
AA Mutation	p.Asp382Asn(p.D382N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173890206:173890206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473T>C
AA Mutation	p.Leu158Ser(p.L158S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173889897:173889897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164G>A
AA Mutation	p.Ser55Asn(p.S55N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265085
Start	173890558:173890558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265085
Start	173890521:173890522(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.789_790delTA
AA Mutation	p.His263GlnfsTer6(p.H263Qfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265085
Start	173953274:173953274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1962+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CPEB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173889828:173889828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95A>G
AA Mutation	p.His32Arg(p.H32R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173949528:173949528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1477C>T
AA Mutation	p.Arg493Cys(p.R493C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265085
Start	173889740:173889740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7G>A
AA Mutation	p.Asp3Asn(p.D3N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000265085
Start	173945098:173945098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414C>T
AA Mutation	p.Arg472Ter(p.R472*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript