Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CCNE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308108
Start	94892852:94892852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754771951
CDS Mutation	c.283C>A
AA Mutation	p.Leu95Ile(p.L95I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308108
Start	94882184:94882184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049C>A
AA Mutation	p.Pro350His(p.P350H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308108
Start	94882872:94882872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308108
Start	94893932:94893932(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.124delA
AA Mutation	p.Arg42GlufsTer38(p.R42Efs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308108
Start	94890508:94890509(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.359dupA
AA Mutation	p.Glu121GlyfsTer7(p.E121Gfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCNE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308108
Start	94893920:94893920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136G>A
AA Mutation	p.Val46Ile(p.V46I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308108
Start	94882886:94882886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838G>T
AA Mutation	p.Asp280Tyr(p.D280Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308108
Start	94892960:94892960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175C>T
AA Mutation	p.Pro59Ser(p.P59S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308108
Start	94893931:94893932(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.124dupA
AA Mutation	p.Arg42LysfsTer12(p.R42Kfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000308108
Start	94887912:94887928(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.599_600+15delAGGTAAGTTCTTAAAAG
Mutation Classification	Splice_Site
Feature Type	Transcript