Colon Cancer: Gene >> OCLN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355237
Start	69509262:69509262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172T>A
AA Mutation	p.Trp58Arg(p.W58R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355237
Start	69509340:69509340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>A
AA Mutation	p.Ala84Thr(p.A84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355237
Start	69509215:69509215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125C>T
AA Mutation	p.Pro42Leu(p.P42L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355237
Start	69509618:69509618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.528A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355237
Start	69513962:69513962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.744A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355237
Start	69545084:69545084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767324023
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355237
Start	69509380:69509380(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.293delT
AA Mutation	p.Leu98Ter(p.L98*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355237
Start	69504282:69504282(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.39delG
AA Mutation	p.Arg13SerfsTer52(p.R13Sfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000355237
Start	69509602:69509603(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.512_513insGC
AA Mutation	p.Tyr171Ter(p.Y171*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OCLN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355237
Start	69514098:69514098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>A
AA Mutation	p.Val294Ile(p.V294I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000355237
Start	69548042:69548042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366G>T
AA Mutation	p.Glu456Ter(p.E456*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript