Colon Cancer: Gene >> CEP55

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371485
Start	93517171:93517171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916A>C
AA Mutation	p.Lys306Gln(p.K306Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371485
Start	93515500:93515500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624A>C
AA Mutation	p.Lys208Asn(p.K208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371485
Start	93515493:93515493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.617A>G
AA Mutation	p.Glu206Gly(p.E206G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371485
Start	93503231:93503231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302T>C
AA Mutation	p.Leu101Pro(p.L101P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371485
Start	93517052:93517052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749800886
CDS Mutation	c.797G>A
AA Mutation	p.Arg266Gln(p.R266Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371485
Start	93503252:93503252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323C>G
AA Mutation	p.Thr108Arg(p.T108R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371485
Start	93503208:93503208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371485
Start	93516987:93516987(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.738delA
AA Mutation	p.Asp247IlefsTer9(p.D247Ifs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000371485
Start	93503296:93503297(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.367_368insTGAGTTGAT
AA Mutation	p.Glu123delinsValSerTerTer(p.E123delinsVS**)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CEP55

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371485
Start	93503145:93503145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216G>T
AA Mutation	p.Lys72Asn(p.K72N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371485
Start	93519720:93519720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370915787
CDS Mutation	c.1104C>T
Mutation Classification	Silent
Feature Type	Transcript