Mutation

Primary Site >> Stomach Cancer

Gene >> NOTCH1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136510773:136510773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776698364
CDS Mutation	c.2620G>A
AA Mutation	p.Val874Ile(p.V874I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136500805:136500805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5681G>A
AA Mutation	p.Gly1894Asp(p.G1894D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136517317:136517317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752071569
CDS Mutation	c.1510C>T
AA Mutation	p.Arg504Cys(p.R504C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136508237:136508237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756087913
CDS Mutation	c.3320G>A
AA Mutation	p.Arg1107Gln(p.R1107Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136517916:136517916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528033027
CDS Mutation	c.1277C>T
AA Mutation	p.Ala426Val(p.A426V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136500676:136500676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5810G>A
AA Mutation	p.Arg1937His(p.R1937H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136503323:136503323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5026G>A
AA Mutation	p.Val1676Ile(p.V1676I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136496199:136496199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7540C>A
AA Mutation	p.Pro2514Thr(p.P2514T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136507428:136507428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3520G>A
AA Mutation	p.Gly1174Ser(p.G1174S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136496819:136496819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6920A>G
AA Mutation	p.Gln2307Arg(p.Q2307R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136500766:136500766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5720C>T
AA Mutation	p.Pro1907Leu(p.P1907L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136501772:136501772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5614A>G
AA Mutation	p.Met1872Val(p.M1872V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136505009:136505009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4682G>A
AA Mutation	p.Cys1561Tyr(p.C1561Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136509854:136509854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2848G>A
AA Mutation	p.Ala950Thr(p.A950T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136523956:136523956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164C>T
AA Mutation	p.Pro55Leu(p.P55L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136500601:136500601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5885G>A
AA Mutation	p.Arg1962His(p.R1962H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136496627:136496627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7112C>G
AA Mutation	p.Thr2371Ser(p.T2371S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136498928:136498928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6151G>T
AA Mutation	p.Gly2051Trp(p.G2051W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136506868:136506868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3749G>A
AA Mutation	p.Gly1250Asp(p.G1250D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136517800:136517800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393G>A
AA Mutation	p.Ala465Thr(p.A465T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136497264:136497264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371742334
CDS Mutation	c.6475C>T
AA Mutation	p.Arg2159Cys(p.R2159C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136511215:136511215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2524G>T
AA Mutation	p.Gly842Trp(p.G842W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136500721:136500721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765708087
CDS Mutation	c.5765A>G
AA Mutation	p.Asn1922Ser(p.N1922S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136513045:136513045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2443T>C
AA Mutation	p.Cys815Arg(p.C815R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136509793:136509793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571425395
CDS Mutation	c.2909C>T
AA Mutation	p.Thr970Ile(p.T970I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136506952:136506952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3665T>C
AA Mutation	p.Val1222Ala(p.V1222A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136515513:136515513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1873T>G
AA Mutation	p.Tyr625Asp(p.Y625D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000277541
Start	136496724:136496724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7015G>A
AA Mutation	p.Ala2339Thr(p.A2339T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136497418:136497418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532201830
CDS Mutation	c.6321C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136502283:136502283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777013344
CDS Mutation	c.5373C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136505600:136505600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774697636
CDS Mutation	c.4296C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136505852:136505852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4044C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136518156:136518156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780769573
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136497325:136497325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750732295
CDS Mutation	c.6414G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136503195:136503195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755764089
CDS Mutation	c.5154C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136517927:136517927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136506599:136506599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3942G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136510762:136510762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777573424
CDS Mutation	c.2631G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136501755:136501755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35627681
CDS Mutation	c.5631C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136497355:136497355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746762310
CDS Mutation	c.6384G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277541
Start	136513124:136513124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2364C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000277541
Start	136496284:136496284(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7455delC
AA Mutation	p.Ser2486ArgfsTer103(p.S2486Rfs*103)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000277541
Start	136496719:136496719(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7020delC
AA Mutation	p.Ser2341ProfsTer7(p.S2341Pfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000277541
Start	136515622:136515622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1764delC
AA Mutation	p.Cys589AlafsTer42(p.C589Afs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000277541
Start	136514602:136514602(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2115delC
AA Mutation	p.Glu706ArgfsTer66(p.E706Rfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	46
Mutation Consequence	stop_gained
Transcription ID	ENST00000277541
Start	136517869:136517869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324C>T
AA Mutation	p.Gln442Ter(p.Q442*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	47
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000277541
Start	136515402:136515402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1904-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript