Colon Cancer: Gene >> CPEB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82556013:82556013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716C>A
AA Mutation	p.Ala239Asp(p.A239D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82553896:82553896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.955C>T
AA Mutation	p.Pro319Ser(p.P319S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82547228:82547228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1409G>A
AA Mutation	p.Arg470His(p.R470H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82553956:82553956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895C>A
AA Mutation	p.Leu299Ile(p.L299I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82544641:82544641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1637G>A
AA Mutation	p.Arg546His(p.R546H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82553895:82553895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.956C>T
AA Mutation	p.Pro319Leu(p.P319L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82549609:82549609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250C>T
AA Mutation	p.Pro417Leu(p.P417L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82553530:82553530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000T>G
AA Mutation	p.Phe334Val(p.F334V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82547229:82547229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1408C>T
AA Mutation	p.Arg470Cys(p.R470C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82571464:82571464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200188266
CDS Mutation	c.259C>T
AA Mutation	p.Arg87Cys(p.R87C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000615198
Start	82549572:82549572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758545052
CDS Mutation	c.1287C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000615198
Start	82549482:82549482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1377A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000615198
Start	82627283:82627283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100C>T
AA Mutation	p.Arg34Ter(p.R34*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000615198
Start	82546449:82546449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567C>T
AA Mutation	p.Arg523Ter(p.R523*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CPEB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82571463:82571463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260G>A
AA Mutation	p.Arg87His(p.R87H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82544601:82544601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1677T>G
AA Mutation	p.Asp559Glu(p.D559E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82547229:82547229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1408C>A
AA Mutation	p.Arg470Ser(p.R470S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82556037:82556037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692C>A
AA Mutation	p.Ser231Tyr(p.S231Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000615198
Start	82571413:82571413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310C>A
AA Mutation	p.Leu104Met(p.L104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript