Mutation

Primary Site >> Stomach Cancer

Gene >> ROBO1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	79125472:79125472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156T>G
AA Mutation	p.Asn52Lys(p.N52K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000464233
Start	78633935:78633935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3481G>T
AA Mutation	p.Gly1161Trp(p.G1161W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78688745:78688745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377297596
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358His(p.R358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78606945:78606945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4532T>C
AA Mutation	p.Leu1511Pro(p.L1511P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	79125477:79125477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151G>A
AA Mutation	p.Asp51Asn(p.D51N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78717341:78717341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851A>G
AA Mutation	p.Glu284Gly(p.E284G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78746870:78746870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754092395
CDS Mutation	c.530C>T
AA Mutation	p.Ser177Leu(p.S177L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78717339:78717339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853G>A
AA Mutation	p.Ala285Thr(p.A285T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78685782:78685782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306A>C
AA Mutation	p.Ser436Arg(p.S436R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78600133:78600133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4921G>T
AA Mutation	p.Asp1641Tyr(p.D1641Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78746816:78746816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>T
AA Mutation	p.Arg195Leu(p.R195L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78607027:78607027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4450C>T
AA Mutation	p.Pro1484Ser(p.P1484S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78631179:78631179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3608A>G
AA Mutation	p.Asn1203Ser(p.N1203S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78714450:78714450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992T>C
AA Mutation	p.Val331Ala(p.V331A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78617970:78617970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3947G>T
AA Mutation	p.Gly1316Val(p.G1316V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78606815:78606815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4662G>T
AA Mutation	p.Gln1554His(p.Q1554H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78631290:78631290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3497A>T
AA Mutation	p.Lys1166Met(p.K1166M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78639800:78639800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2981G>A
AA Mutation	p.Cys994Tyr(p.C994Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78606783:78606783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4694A>G
AA Mutation	p.Asn1565Ser(p.N1565S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78938921:78938921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179G>T
AA Mutation	p.Arg60Leu(p.R60L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78685797:78685797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291T>G
AA Mutation	p.Leu431Val(p.L431V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78717377:78717377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815C>A
AA Mutation	p.Ala272Glu(p.A272E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78635832:78635832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3314A>G
AA Mutation	p.Gln1105Arg(p.Q1105R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78938907:78938907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.193G>T
AA Mutation	p.Asp65Tyr(p.D65Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78631279:78631279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3508A>G
AA Mutation	p.Arg1170Gly(p.R1170G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78636097:78636097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3049G>T
AA Mutation	p.Ala1017Ser(p.A1017S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78938894:78938894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377370843
CDS Mutation	c.206G>A
AA Mutation	p.Arg69His(p.R69H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000464233
Start	78651780:78651780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767615237
CDS Mutation	c.2764C>T
AA Mutation	p.Arg922Cys(p.R922C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000464233
Start	78635819:78635819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3327G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000464233
Start	78617699:78617699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4218A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000464233
Start	78600181:78600181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4873A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000464233
Start	78635927:78635927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3219C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000464233
Start	78614781:78614781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558087386
CDS Mutation	c.4302G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000464233
Start	78600137:78600137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4917A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000464233
Start	78661085:78661085(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2265delT
AA Mutation	p.Phe755LeufsTer28(p.F755Lfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000464233
Start	78617724:78617724(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4193delT
AA Mutation	p.Phe1398SerfsTer19(p.F1398Sfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000464233
Start	78746880:78746880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520C>T
AA Mutation	p.Gln174Ter(p.Q174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000464233
Start	78714514:78714514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Ter(p.R310*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000464233
Start	78667886:78667886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963C>T
AA Mutation	p.Gln655Ter(p.Q655*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000464233
Start	78607040:78607041(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4436_4437insACAACCTG
AA Mutation	p.Asp1479GlufsTer15(p.D1479Efs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000464233
Start	78647631:78647632(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2836dupA
AA Mutation	p.Thr946AsnfsTer24(p.T946Nfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	42
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000464233
Start	78614646:78614646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4435+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript