Mutation

Primary Site >> Stomach Cancer

Gene >> ROBO2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77644844:77644844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776990102
CDS Mutation	c.4075G>A
AA Mutation	p.Asp1359Asn(p.D1359N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77481115:77481115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563T>C
AA Mutation	p.Leu188Pro(p.L188P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77574644:77574644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2117T>G
AA Mutation	p.Val706Gly(p.V706G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77602446:77602446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3091A>T
AA Mutation	p.Met1031Leu(p.M1031L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000461745
Start	77607953:77607953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3292G>T
AA Mutation	p.Gly1098Cys(p.G1098C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77596646:77596646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2750G>T
AA Mutation	p.Gly917Val(p.G917V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77644725:77644725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3956G>T
AA Mutation	p.Ser1319Ile(p.S1319I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77565027:77565027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753772733
CDS Mutation	c.1756C>T
AA Mutation	p.Arg586Trp(p.R586W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77634909:77634909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3800G>T
AA Mutation	p.Ser1267Ile(p.S1267I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77644812:77644812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4043T>C
AA Mutation	p.Val1348Ala(p.V1348A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77550905:77550905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Cys(p.R383C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77098188:77098188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236G>A
AA Mutation	p.Arg79Gln(p.R79Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77565061:77565061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762706045
CDS Mutation	c.1790C>T
AA Mutation	p.Ala597Val(p.A597V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77622342:77622342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3670G>A
AA Mutation	p.Glu1224Lys(p.E1224K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77580010:77580010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2392T>A
AA Mutation	p.Ser798Thr(p.S798T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77634989:77634989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3880G>T
AA Mutation	p.Gly1294Trp(p.G1294W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77546410:77546410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007A>G
AA Mutation	p.Glu336Gly(p.E336G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77557988:77557988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276A>G
AA Mutation	p.Asn426Asp(p.N426D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77617628:77617628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372515749
CDS Mutation	c.3409G>A
AA Mutation	p.Val1137Met(p.V1137M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77098121:77098121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778332221
CDS Mutation	c.169C>T
AA Mutation	p.Arg57Trp(p.R57W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77098095:77098095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751711354
CDS Mutation	c.143C>T
AA Mutation	p.Thr48Met(p.T48M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000461745
Start	77568433:77568433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756826211
CDS Mutation	c.1970C>T
AA Mutation	p.Thr657Met(p.T657M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77568373:77568373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910T>C
AA Mutation	p.Val637Ala(p.V637A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77574577:77574577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2050T>C
AA Mutation	p.Trp684Arg(p.W684R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77617592:77617592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3373G>T
AA Mutation	p.Asp1125Tyr(p.D1125Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77477516:77477516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491C>G
AA Mutation	p.Thr164Ser(p.T164S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77607896:77607896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3235G>A
AA Mutation	p.Val1079Ile(p.V1079I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77574721:77574721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2194A>G
AA Mutation	p.Thr732Ala(p.T732A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000461745
Start	77644839:77644839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761197885
CDS Mutation	c.4070C>T
AA Mutation	p.Ala1357Val(p.A1357V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77558146:77558146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77563300:77563300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1653A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77098324:77098324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763736763
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77558089:77558089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77522898:77522898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77617555:77617555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3336T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77098135:77098135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77574552:77574552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2025T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77493323:77493323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77622341:77622341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2272164
CDS Mutation	c.3669C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000461745
Start	77617627:77617627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143561771
CDS Mutation	c.3408C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000461745
Start	77098184:77098184(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.235delC
AA Mutation	p.Arg79GlyfsTer42(p.R79Gfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000461745
Start	77568410:77568419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1949_1958delCCACGGTTCA
AA Mutation	p.Thr650ArgfsTer18(p.T650Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000461745
Start	77634974:77634974(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3870delA
AA Mutation	p.Lys1290AsnfsTer20(p.K1290Nfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	44
Mutation Consequence	stop_gained
Transcription ID	ENST00000461745
Start	77617622:77617622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3403C>T
AA Mutation	p.Arg1135Ter(p.R1135*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	45
Mutation Consequence	stop_gained
Transcription ID	ENST00000461745
Start	77635022:77635022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3913C>T
AA Mutation	p.Arg1305Ter(p.R1305*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	46
Mutation Consequence	stop_gained
Transcription ID	ENST00000461745
Start	77477525:77477525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Trp167Ter(p.W167*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript