Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAGI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65361241:65361241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201117026
CDS Mutation	c.3592C>T
AA Mutation	p.Arg1198Cys(p.R1198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65429922:65429922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1765T>A
AA Mutation	p.Tyr589Asn(p.Y589N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	66038031:66038031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278G>A
AA Mutation	p.Cys93Tyr(p.C93Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65381957:65381957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2621A>T
AA Mutation	p.Gln874Leu(p.Q874L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65357074:65357074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3693G>T
AA Mutation	p.Arg1231Ser(p.R1231S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65379437:65379437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757905500
CDS Mutation	c.2819C>T
AA Mutation	p.Thr940Met(p.T940M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356835:65356835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3932G>A
AA Mutation	p.Arg1311His(p.R1311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356833:65356833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778933016
CDS Mutation	c.3934G>A
AA Mutation	p.Ala1312Thr(p.A1312T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65478738:65478738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611C>T
AA Mutation	p.Thr204Met(p.T204M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65430818:65430818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375653415
CDS Mutation	c.1427G>A
AA Mutation	p.Arg476Gln(p.R476Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65391193:65391193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770193154
CDS Mutation	c.2365C>A
AA Mutation	p.Pro789Thr(p.P789T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65364884:65364884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3259A>C
AA Mutation	p.Thr1087Pro(p.T1087P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65430026:65430026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776804460
CDS Mutation	c.1661G>A
AA Mutation	p.Arg554Gln(p.R554Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65493524:65493524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538G>A
AA Mutation	p.Gly180Ser(p.G180S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356770:65356770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142375705
CDS Mutation	c.3997G>A
AA Mutation	p.Ala1333Thr(p.A1333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65401443:65401443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2195A>C
AA Mutation	p.Lys732Thr(p.K732T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356902:65356902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3865C>T
AA Mutation	p.Pro1289Ser(p.P1289S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356775:65356775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3992G>A
AA Mutation	p.Arg1331His(p.R1331H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65470409:65470409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>T
AA Mutation	p.Ala278Val(p.A278V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65429591:65429591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2096A>G
AA Mutation	p.His699Arg(p.H699R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65379312:65379312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2944G>A
AA Mutation	p.Gly982Ser(p.G982S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65356728:65356728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4039C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65379301:65379301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2955C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65356825:65356825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141542625
CDS Mutation	c.3942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65375857:65375857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3084C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65439928:65439928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs62642828
CDS Mutation	c.1221A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65439901:65439901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65381980:65381980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2598G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402939
Start	66038221:66038221(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.88delG
AA Mutation	p.Val30Ter(p.V30*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000402939
Start	65356694:65356694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4073C>A
AA Mutation	p.Ser1358Ter(p.S1358*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000402939
Start	65429526:65429526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2161C>T
AA Mutation	p.Arg721Ter(p.R721*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAGI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65391193:65391193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770193154
CDS Mutation	c.2365C>A
AA Mutation	p.Pro789Thr(p.P789T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356910:65356910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3857C>T
AA Mutation	p.Ser1286Leu(p.S1286L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65364919:65364919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3224A>G
AA Mutation	p.Asn1075Ser(p.N1075S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65361241:65361241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201117026
CDS Mutation	c.3592C>T
AA Mutation	p.Arg1198Cys(p.R1198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65429798:65429798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1889C>A
AA Mutation	p.Ser630Tyr(p.S630Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65391146:65391146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2412C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65622030:65622030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000402939
Start	66038276:66038276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33G>A
AA Mutation	p.Trp11Ter(p.W11*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript