Mutation

Primary Site >> Stomach Cancer

Gene >> NOTCH3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15170547:15170547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375474414
CDS Mutation	c.4898C>T
AA Mutation	p.Pro1633Leu(p.P1633L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15162541:15162541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5837C>T
AA Mutation	p.Ala1946Val(p.A1946V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15170508:15170508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4937T>G
AA Mutation	p.Leu1646Arg(p.L1646R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15192161:15192161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478G>T
AA Mutation	p.Asp160Tyr(p.D160Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15170448:15170448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4997G>A
AA Mutation	p.Arg1666Gln(p.R1666Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15187255:15187255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374767079
CDS Mutation	c.1690G>A
AA Mutation	p.Ala564Thr(p.A564T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15165936:15165936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5518G>A
AA Mutation	p.Glu1840Lys(p.E1840K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15167288:15167288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139983430
CDS Mutation	c.5323G>A
AA Mutation	p.Ala1775Thr(p.A1775T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15191793:15191793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115836330
CDS Mutation	c.754G>A
AA Mutation	p.Val252Met(p.V252M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15179097:15179097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3646G>A
AA Mutation	p.Ala1216Thr(p.A1216T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15178884:15178884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3776G>A
AA Mutation	p.Gly1259Asp(p.G1259D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15188328:15188328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399G>A
AA Mutation	p.Glu467Lys(p.E467K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15167318:15167318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5293G>A
AA Mutation	p.Ala1765Thr(p.A1765T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263388
Start	15165515:15165515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5668A>G
AA Mutation	p.Ile1890Val(p.I1890V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15180100:15180100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189545202
CDS Mutation	c.3299G>A
AA Mutation	p.Arg1100His(p.R1100H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15185371:15185371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2182C>T
AA Mutation	p.Arg728Cys(p.R728C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15181011:15181011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2944C>T
AA Mutation	p.Pro982Ser(p.P982S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15170439:15170439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5006G>A
AA Mutation	p.Arg1669His(p.R1669H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15192151:15192151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761209241
CDS Mutation	c.488G>A
AA Mutation	p.Arg163Gln(p.R163Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000263388
Start	15170356:15170356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5089G>A
AA Mutation	p.Val1697Met(p.V1697M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263388
Start	15191644:15191644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780139667
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263388
Start	15191779:15191779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778247982
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263388
Start	15200801:15200801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263388
Start	15170390:15170390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763442658
CDS Mutation	c.5055C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263388
Start	15160890:15160890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6738C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263388
Start	15179170:15179170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3573C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263388
Start	15166077:15166077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5377C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263388
Start	15185547:15185547(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2084delC
AA Mutation	p.Pro695ArgfsTer165(p.P695Rfs*165)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263388
Start	15192010:15192010(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.629delG
AA Mutation	p.Gly210AlafsTer26(p.G210Afs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263388
Start	15179159:15179159(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3584delC
AA Mutation	p.Pro1195GlnfsTer77(p.P1195Qfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263388
Start	15180085:15180085(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3314delG
AA Mutation	p.Gly1105AlafsTer167(p.G1105Afs*167)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263388
Start	15162495:15162496(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5882dupA
AA Mutation	p.Asn1961LysfsTer5(p.N1961Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript