Colon Cancer: Gene >> BOP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000569669
Start	144264930:144264930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532G>A
AA Mutation	p.Asp178Asn(p.D178N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000569669
Start	144289250:144289250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782267874
CDS Mutation	c.154G>A
AA Mutation	p.Val52Ile(p.V52I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000569669
Start	144263709:144263709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1274G>A
AA Mutation	p.Gly425Asp(p.G425D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000569669
Start	144262177:144262177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2228G>A
AA Mutation	p.Arg743His(p.R743H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000569669
Start	144264761:144264761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616C>T
AA Mutation	p.Arg206Trp(p.R206W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000569669
Start	144262235:144262235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2170G>A
AA Mutation	p.Val724Ile(p.V724I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000569669
Start	144289294:144289294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110T>A
AA Mutation	p.Leu37His(p.L37H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000569669
Start	144263600:144263600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000569669
Start	144264354:144264354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000569669
Start	144289298:144289298(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs782769521
CDS Mutation	c.106delC
AA Mutation	p.Leu36SerfsTer154(p.L36Sfs*154)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BOP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000569669
Start	144264320:144264320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.883C>T
AA Mutation	p.Arg295Cys(p.R295C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript