Colon Cancer: Gene >> EPHA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221456750:221456750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1466G>C
AA Mutation	p.Arg489Pro(p.R489P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221434177:221434177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2461G>A
AA Mutation	p.Gly821Arg(p.G821R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221442988:221442988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1915C>T
AA Mutation	p.Arg639Cys(p.R639C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221564151:221564151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Cys(p.R135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221563760:221563760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794G>A
AA Mutation	p.Gly265Glu(p.G265E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221482600:221482600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756184907
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357His(p.R357H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221443543:221443543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1838C>T
AA Mutation	p.Ala613Val(p.A613V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221455583:221455583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1679T>A
AA Mutation	p.Val560Glu(p.V560E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221572223:221572223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26T>C
AA Mutation	p.Leu9Pro(p.L9P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221434288:221434288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2350G>T
AA Mutation	p.Gly784Cys(p.G784C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221446161:221446161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736C>T
AA Mutation	p.Ala579Val(p.A579V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221501079:221501079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537081277
CDS Mutation	c.917C>T
AA Mutation	p.Ser306Leu(p.S306L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221456709:221456709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507C>A
AA Mutation	p.Leu503Met(p.L503M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281821
Start	221482650:221482650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147516232
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281821
Start	221563792:221563792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281821
Start	221563821:221563821(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.733delA
AA Mutation	p.Met245CysfsTer89(p.M245Cfs*89)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221564301:221564301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253C>T
AA Mutation	p.Arg85Ter(p.R85*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221443553:221443553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828C>T
AA Mutation	p.Arg610Ter(p.R610*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221457958:221457958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1351G>T
AA Mutation	p.Glu451Ter(p.E451*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281821
Start	221430113:221430114(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2534dupC
AA Mutation	p.Pro846SerfsTer25(p.P846Sfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281821
Start	221564362:221564363(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.191dupA
AA Mutation	p.Asn64LysfsTer19(p.N64Kfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000281821
Start	221455613:221455615(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1647_1649delTCT
AA Mutation	p.Leu550del(p.L550del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EPHA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221429976:221429976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2672C>T
AA Mutation	p.Thr891Ile(p.T891I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221482580:221482580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>A
AA Mutation	p.Val364Met(p.V364M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221456742:221456742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1474C>T
AA Mutation	p.Arg492Trp(p.R492W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221563956:221563956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598T>C
AA Mutation	p.Phe200Leu(p.F200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281821
Start	221455645:221455645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1617C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221501089:221501089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>T
AA Mutation	p.Gly303Ter(p.G303*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript