Mutation

Primary Site >> Stomach Cancer

Gene >> ROS1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117300985:117300985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6722A>G
AA Mutation	p.Glu2241Gly(p.E2241G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117321354:117321354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5682A>T
AA Mutation	p.Glu1894Asp(p.E1894D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117341596:117341596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141448347
CDS Mutation	c.4706G>A
AA Mutation	p.Arg1569Gln(p.R1569Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117341214:117341214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5000C>T
AA Mutation	p.Pro1667Leu(p.P1667L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117362670:117362670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3314A>T
AA Mutation	p.Asn1105Ile(p.N1105I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117386897:117386897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2117A>T
AA Mutation	p.Asn706Ile(p.N706I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117353045:117353045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4266G>T
AA Mutation	p.Lys1422Asn(p.K1422N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117319888:117319888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5920G>A
AA Mutation	p.Glu1974Lys(p.E1974K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117326382:117326382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5399A>C
AA Mutation	p.Asn1800Thr(p.N1800T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368508
Start	117396915:117396915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Lys(p.R260K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117288769:117288769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6767A>G
AA Mutation	p.Asp2256Gly(p.D2256G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117310092:117310092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6423A>C
AA Mutation	p.Gln2141His(p.Q2141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117365630:117365630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2924T>C
AA Mutation	p.Val975Ala(p.V975A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117389767:117389767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1342C>G
AA Mutation	p.Arg448Gly(p.R448G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117311110:117311110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6143G>A
AA Mutation	p.Gly2048Asp(p.G2048D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117360003:117360003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3454C>A
AA Mutation	p.Pro1152Thr(p.P1152T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117366229:117366229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2659G>T
AA Mutation	p.Ala887Ser(p.A887S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117310228:117310228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6287G>A
AA Mutation	p.Arg2096Gln(p.R2096Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117365633:117365633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759586931
CDS Mutation	c.2921C>T
AA Mutation	p.Ala974Val(p.A974V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117311054:117311054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6199T>G
AA Mutation	p.Cys2067Gly(p.C2067G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117359882:117359882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3575A>T
AA Mutation	p.Asp1192Val(p.D1192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000368508
Start	117389829:117389829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1280T>C
AA Mutation	p.Leu427Pro(p.L427P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368508
Start	117319925:117319925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5883A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368508
Start	117301116:117301116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6591C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368508
Start	117403263:117403263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777706763
CDS Mutation	c.453G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368508
Start	117341403:117341403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4899A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368508
Start	117389522:117389522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527529345
CDS Mutation	c.1587C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368508
Start	117387877:117387877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1917G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368508
Start	117393246:117393246(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1240delA
AA Mutation	p.Ile414LeufsTer14(p.I414Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368508
Start	117344088:117344088(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4496delA
AA Mutation	p.Asn1499ThrfsTer5(p.N1499Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000368508
Start	117337211:117337211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5209G>T
AA Mutation	p.Glu1737Ter(p.E1737*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000368508
Start	117386925:117386925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2089G>T
AA Mutation	p.Gly697Ter(p.G697*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000368508
Start	117329363:117329363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5332G>T
AA Mutation	p.Gly1778Ter(p.G1778*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368508
Start	117394238:117394239(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1087dupT
AA Mutation	p.Tyr363LeufsTer25(p.Y363Lfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368508
Start	117301041:117301042(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6665dupT
AA Mutation	p.Asn2224LysfsTer2(p.N2224Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript