Colon Cancer: Gene >> PPP2R5E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337537
Start	63539676:63539676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10G>A
AA Mutation	p.Ala4Thr(p.A4T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337537
Start	63539679:63539679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7T>C
AA Mutation	p.Ser3Pro(p.S3P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337537
Start	63453712:63453712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331A>G
AA Mutation	p.Thr111Ala(p.T111A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337537
Start	63396652:63396652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614G>T
AA Mutation	p.Arg205Ile(p.R205I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337537
Start	63453806:63453806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337537
Start	63376066:63376066(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1347delA
AA Mutation	p.Lys449AsnfsTer7(p.K449Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337537
Start	63396665:63396665(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.601delA
AA Mutation	p.Thr201GlnfsTer26(p.T201Qfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPP2R5E

No Mutation Annotation!