Mutation

Primary Site >> Stomach Cancer

Gene >> TIE1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43318023:43318023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751919729
CDS Mutation	c.2873G>A
AA Mutation	p.Arg958His(p.R958H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43307216:43307216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771302065
CDS Mutation	c.715G>A
AA Mutation	p.Asp239Asn(p.D239N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43313342:43313342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135C>T
AA Mutation	p.Thr712Met(p.T712M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43308989:43308989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046G>A
AA Mutation	p.Arg349Gln(p.R349Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43309479:43309479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550355457
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427His(p.R427H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43317903:43317903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2753A>G
AA Mutation	p.Glu918Gly(p.E918G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43317341:43317341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2552G>T
AA Mutation	p.Gly851Val(p.G851V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43309439:43309439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240C>T
AA Mutation	p.Pro414Ser(p.P414S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43312308:43312308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634C>A
AA Mutation	p.Pro545His(p.P545H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43307921:43307921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039T>C
AA Mutation	p.Ser347Pro(p.S347P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43317896:43317896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2746G>A
AA Mutation	p.Ala916Thr(p.A916T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43318038:43318038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369292846
CDS Mutation	c.2888C>T
AA Mutation	p.Ala963Val(p.A963V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43311697:43311697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759402690
CDS Mutation	c.1360C>T
AA Mutation	p.Arg454Trp(p.R454W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43312433:43312433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770948609
CDS Mutation	c.1759G>A
AA Mutation	p.Gly587Arg(p.G587R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372476
Start	43307572:43307572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913G>T
AA Mutation	p.Ala305Ser(p.A305S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43313150:43313150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777663496
CDS Mutation	c.1943G>A
AA Mutation	p.Arg648Gln(p.R648Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43305063:43305063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767336788
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Cys(p.R91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43313942:43313942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2383C>A
AA Mutation	p.Arg795Ser(p.R795S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43305135:43305135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Cys(p.R115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43309442:43309442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200415018
CDS Mutation	c.1243C>T
AA Mutation	p.Arg415Cys(p.R415C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43309392:43309392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193C>T
AA Mutation	p.Thr398Ile(p.T398I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43307524:43307524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865T>C
AA Mutation	p.Tyr289His(p.Y289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000372476
Start	43311698:43311698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771606371
CDS Mutation	c.1361G>A
AA Mutation	p.Arg454Gln(p.R454Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43308990:43308990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43312432:43312432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201759080
CDS Mutation	c.1758C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43307212:43307212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43304957:43304957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43312570:43312570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781170758
CDS Mutation	c.1896G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372476
Start	43311798:43311798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372476
Start	43307239:43307239(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.743delC
AA Mutation	p.Pro248LeufsTer117(p.P248Lfs*117)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372476
Start	43301087:43301087(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.20delC
AA Mutation	p.Pro7LeufsTer19(p.P7Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372476
Start	43313144:43313144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1942delC
AA Mutation	p.Arg648AspfsTer15(p.R648Dfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000372476
Start	43313149:43313149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1942C>T
AA Mutation	p.Arg648Ter(p.R648*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000372476
Start	43312603:43312603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1927+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript