Mutation

Primary Site >> Stomach Cancer

Gene >> NOTCH4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32201220:32201220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4036C>T
AA Mutation	p.Arg1346Trp(p.R1346W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32217185:32217185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1706A>G
AA Mutation	p.Gln569Arg(p.Q569R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32198986:32198986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761314959
CDS Mutation	c.4475G>A
AA Mutation	p.Arg1492Gln(p.R1492Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32202221:32202221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3610T>C
AA Mutation	p.Ser1204Pro(p.S1204P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32220771:32220771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907C>A
AA Mutation	p.Pro303Thr(p.P303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32200917:32200917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143040647
CDS Mutation	c.4229G>A
AA Mutation	p.Arg1410His(p.R1410H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32195777:32195777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5672G>C
AA Mutation	p.Gly1891Ala(p.G1891A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32198959:32198959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4502G>A
AA Mutation	p.Arg1501Gln(p.R1501Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32220777:32220777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.901C>T
AA Mutation	p.Leu301Phe(p.L301F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32197051:32197051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5074A>G
AA Mutation	p.Thr1692Ala(p.T1692A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32201459:32201459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3797G>A
AA Mutation	p.Gly1266Glu(p.G1266E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32222765:32222765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197A>G
AA Mutation	p.Asp66Gly(p.D66G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32195835:32195835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs8192582
CDS Mutation	c.5614G>A
AA Mutation	p.Gly1872Arg(p.G1872R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32196334:32196334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5288A>G
AA Mutation	p.Gln1763Arg(p.Q1763R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32221308:32221308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762851866
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Trp(p.R157W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32202311:32202311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775047010
CDS Mutation	c.3520G>A
AA Mutation	p.Gly1174Arg(p.G1174R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32197414:32197414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748941744
CDS Mutation	c.4937G>A
AA Mutation	p.Arg1646Gln(p.R1646Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32219714:32219714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1388G>A
AA Mutation	p.Cys463Tyr(p.C463Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000375023
Start	32198963:32198963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4498C>T
AA Mutation	p.Arg1500Cys(p.R1500C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32204237:32204237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774972771
CDS Mutation	c.3018C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32221213:32221213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765731164
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32202141:32202141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3690C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32220175:32220175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32198940:32198940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4521C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32198946:32198946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752383712
CDS Mutation	c.4515C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32204231:32204231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776017114
CDS Mutation	c.3024C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32202153:32202153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3678C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375023
Start	32202102:32202102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780232367
CDS Mutation	c.3729C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375023
Start	32210858:32210858(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs761063325
CDS Mutation	c.2759delC
AA Mutation	p.Pro920LeufsTer12(p.P920Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375023
Start	32195513:32195513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5936delG
AA Mutation	p.Gly1979AspfsTer17(p.G1979Dfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375023
Start	32202370:32202370(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3461delG
AA Mutation	p.Gly1154AlafsTer150(p.G1154Afs*150)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375023
Start	32197548:32197549(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4801_4802dupCA
AA Mutation	p.Gln1601HisfsTer106(p.Q1601Hfs*106)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript