Colon Cancer: Gene >> BACE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330333
Start	41275401:41275401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1334C>T
AA Mutation	p.Ser445Phe(p.S445F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330333
Start	41243400:41243400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772T>G
AA Mutation	p.Leu258Val(p.L258V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330333
Start	41241937:41241937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737G>T
AA Mutation	p.Gly246Val(p.G246V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330333
Start	41237550:41237550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>A
AA Mutation	p.Val147Met(p.V147M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330333
Start	41250882:41250882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757902823
CDS Mutation	c.1115G>A
AA Mutation	p.Arg372His(p.R372H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330333
Start	41275488:41275488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559873325
CDS Mutation	c.1421C>T
AA Mutation	p.Ala474Val(p.A474V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330333
Start	41246007:41246007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Cys(p.R310C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330333
Start	41275564:41275564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1497C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330333
Start	41168562:41168562(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775381972
CDS Mutation	c.305delC
AA Mutation	p.Pro102ArgfsTer25(p.P102Rfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BACE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330333
Start	41237623:41237623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512C>A
AA Mutation	p.Thr171Asn(p.T171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330333
Start	41168562:41168562(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775381972
CDS Mutation	c.305delC
AA Mutation	p.Pro102ArgfsTer25(p.P102Rfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript