Colon Cancer: Gene >> FOXM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359843
Start	2859297:2859297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145831539
CDS Mutation	c.1633C>T
AA Mutation	p.Arg545Trp(p.R545W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359843
Start	2868667:2868667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>A
AA Mutation	p.Ala248Thr(p.A248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359843
Start	2868690:2868690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719C>G
AA Mutation	p.Ser240Cys(p.S240C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359843
Start	2868729:2868729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144843550
CDS Mutation	c.680C>T
AA Mutation	p.Ala227Val(p.A227V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359843
Start	2859213:2859213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375821639
CDS Mutation	c.1717G>A
AA Mutation	p.Ala573Thr(p.A573T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359843
Start	2859436:2859436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1494A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359843
Start	2866441:2866441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359843
Start	2859517:2859517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1413A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359843
Start	2873999:2873999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754712516
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359843
Start	2858922:2858922(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2008delC
AA Mutation	p.Glu671AsnfsTer12(p.E671Nfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359843
Start	2859044:2859044(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1886delC
AA Mutation	p.Pro629GlnfsTer4(p.P629Qfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000359843
Start	2872188:2872188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Ter(p.R188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FOXM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359843
Start	2868603:2868603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.806A>C
AA Mutation	p.His269Pro(p.H269P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359843
Start	2864704:2864704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1069A>G
AA Mutation	p.Thr357Ala(p.T357A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000359843
Start	2859437:2859437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1493C>A
AA Mutation	p.Ser498Ter(p.S498*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000359843
Start	2872188:2872188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Ter(p.R188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript