Colon Cancer: Gene >> SBF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9845571:9845571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3104C>A
AA Mutation	p.Ser1035Tyr(p.S1035Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9962040:9962040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1777G>T
AA Mutation	p.Gly593Cys(p.G593C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9858329:9858329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1997A>G
AA Mutation	p.Gln666Arg(p.Q666R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9781595:9781595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5363A>G
AA Mutation	p.His1788Arg(p.H1788R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	10028472:10028472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599C>T
AA Mutation	p.Ala200Val(p.A200V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9992435:9992435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276T>A
AA Mutation	p.Ser426Thr(p.S426T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9795884:9795884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4517C>A
AA Mutation	p.Ser1506Tyr(p.S1506Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9853635:9853635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2441C>A
AA Mutation	p.Ser814Tyr(p.S814Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9962100:9962100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1717C>T
AA Mutation	p.Pro573Ser(p.P573S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9839558:9839558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775391548
CDS Mutation	c.3395G>A
AA Mutation	p.Arg1132His(p.R1132H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9790610:9790610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4644G>A
AA Mutation	p.Met1548Ile(p.M1548I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9968442:9968442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759084094
CDS Mutation	c.1499G>A
AA Mutation	p.Arg500Gln(p.R500Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9842658:9842658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750021823
CDS Mutation	c.3223C>T
AA Mutation	p.Arg1075Cys(p.R1075C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256190
Start	9839521:9839521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256190
Start	9847006:9847006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2884C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256190
Start	9832402:9832402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376295625
CDS Mutation	c.3474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256190
Start	10029858:10029858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256190
Start	9853685:9853686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2390_2391delAT
AA Mutation	p.Tyr797Ter(p.Y797*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256190
Start	9808111:9808111(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4332delA
AA Mutation	p.Glu1445SerfsTer15(p.E1445Sfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000256190
Start	9963841:9963841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642C>T
AA Mutation	p.Gln548Ter(p.Q548*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000256190
Start	9852696:9852696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2590A>T
AA Mutation	p.Arg864Ter(p.R864*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000256190
Start	10031124:10031124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326T>G
AA Mutation	p.Leu109Ter(p.L109*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SBF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9961990:9961990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1827C>G
AA Mutation	p.Asp609Glu(p.D609E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9850053:9850053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2776C>A
AA Mutation	p.Leu926Ile(p.L926I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	9968454:9968454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487T>G
AA Mutation	p.Ile496Ser(p.I496S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256190
Start	10028547:10028547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524C>A
AA Mutation	p.Ser175Tyr(p.S175Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000256190
Start	9785177:9785177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750756174
CDS Mutation	c.5179C>T
AA Mutation	p.Arg1727Ter(p.R1727*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000256190
Start	9832350:9832350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774667470
CDS Mutation	c.3526C>T
AA Mutation	p.Arg1176Ter(p.R1176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript