Colon Cancer: Gene >> CPEB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92091848:92091848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669C>A
AA Mutation	p.Pro557Thr(p.P557T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92239422:92239422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>T
AA Mutation	p.Ala310Val(p.A310V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92091835:92091835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1682G>A
AA Mutation	p.Arg561Gln(p.R561Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92052267:92052267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2042C>T
AA Mutation	p.Pro681Leu(p.P681L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92081477:92081477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1712G>A
AA Mutation	p.Arg571His(p.R571H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92239989:92239989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362A>G
AA Mutation	p.Asp121Gly(p.D121G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92240242:92240242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109T>C
AA Mutation	p.Ser37Pro(p.S37P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92145023:92145023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143773953
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Cys(p.R429C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92192599:92192599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747888308
CDS Mutation	c.1043C>T
AA Mutation	p.Ser348Leu(p.S348L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265997
Start	92192598:92192598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CPEB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265997
Start	92192557:92192557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085A>C
AA Mutation	p.Glu362Ala(p.E362A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	start_lost
Transcription ID	ENST00000265997
Start	92240348:92240348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript