Colon Cancer: Gene >> BCAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395961
Start	54058697:54058697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22C>A
AA Mutation	p.Pro8Thr(p.P8T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395961
Start	53985373:53985373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148582842
CDS Mutation	c.1054G>A
AA Mutation	p.Val352Met(p.V352M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395961
Start	53985496:53985496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931G>T
AA Mutation	p.Ala311Ser(p.A311S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395961
Start	53996004:53996004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138168398
CDS Mutation	c.770C>T
AA Mutation	p.Ala257Val(p.A257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395961
Start	54028485:54028485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395961
Start	53953618:53953618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1494C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395961
Start	54028887:54028887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778133024
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395961
Start	53995028:53995028(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.911delA
AA Mutation	p.Lys304ArgfsTer49(p.K304Rfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395961
Start	53996027:53996027(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.747delA
AA Mutation	p.Glu250LysfsTer31(p.E250Kfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395961
Start	53995974:53995975(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.799_800insCAATA
AA Mutation	p.Gly267AlafsTer16(p.G267Afs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BCAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395961
Start	54028781:54028781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201371925
CDS Mutation	c.334G>A
AA Mutation	p.Ala112Thr(p.A112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript