Colon Cancer: Gene >> BUB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110661667:110661667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752483610
CDS Mutation	c.1132A>G
AA Mutation	p.Thr378Ala(p.T378A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110674148:110674148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.163G>A
AA Mutation	p.Glu55Lys(p.E55K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110672718:110672718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537793951
CDS Mutation	c.365T>A
AA Mutation	p.Leu122His(p.L122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110655759:110655759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1856T>C
AA Mutation	p.Val619Ala(p.V619A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110661789:110661789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548365437
CDS Mutation	c.1010C>T
AA Mutation	p.Ala337Val(p.A337V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110670554:110670554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759283101
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110661670:110661670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1129G>A
AA Mutation	p.Ala377Thr(p.A377T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110641796:110641796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2471A>C
AA Mutation	p.Lys824Thr(p.K824T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110639845:110639845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2959G>A
AA Mutation	p.Asp987Asn(p.D987N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110658709:110658709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310C>A
AA Mutation	p.Ser437Tyr(p.S437Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110661736:110661736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063C>A
AA Mutation	p.Pro355Thr(p.P355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110674163:110674163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143906507
CDS Mutation	c.148G>A
AA Mutation	p.Glu50Lys(p.E50K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110657078:110657078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110650631:110650631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2118C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110666266:110666266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763002902
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110669468:110669468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110658516:110658516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1410C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110641384:110641384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2706T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110653492:110653492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77633848
CDS Mutation	c.1908G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110650691:110650691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2058A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302759
Start	110642126:110642127(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2455dupG
AA Mutation	p.Val819GlyfsTer61(p.V819Gfs*61)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000302759
Start	110641204:110641205(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2784_2785insG
AA Mutation	p.Phe929ValfsTer6(p.F929Vfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BUB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302759
Start	110650749:110650749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000C>T
AA Mutation	p.Ser667Leu(p.S667L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302759
Start	110674087:110674087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224T>G
AA Mutation	p.Phe75Cys(p.F75C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302759
Start	110653492:110653492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77633848
CDS Mutation	c.1908G>A
Mutation Classification	Silent
Feature Type	Transcript