Mutation

Primary Site >> Stomach Cancer

Gene >> EPHB1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135248396:135248396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2577C>A
AA Mutation	p.Asp859Glu(p.D859E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135132912:135132912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56396912
CDS Mutation	c.1160C>T
AA Mutation	p.Thr387Met(p.T387M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	134951655:134951655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408A>C
AA Mutation	p.Lys136Asn(p.K136N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135201627:135201627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2284G>A
AA Mutation	p.Asp762Asn(p.D762N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135248412:135248412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758204492
CDS Mutation	c.2593C>T
AA Mutation	p.Arg865Trp(p.R865W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	134951816:134951816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771145808
CDS Mutation	c.569G>A
AA Mutation	p.Arg190His(p.R190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135248485:135248485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2666A>C
AA Mutation	p.Lys889Thr(p.K889T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	134951698:134951698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451T>G
AA Mutation	p.Phe151Val(p.F151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135201478:135201478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2135A>T
AA Mutation	p.Asn712Ile(p.N712I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135248434:135248434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534330476
CDS Mutation	c.2615C>T
AA Mutation	p.Ala872Val(p.A872V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135132891:135132891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139T>G
AA Mutation	p.Val380Gly(p.V380G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135248467:135248467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186851943
CDS Mutation	c.2648G>A
AA Mutation	p.Arg883Gln(p.R883Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135241190:135241190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779665397
CDS Mutation	c.2389G>A
AA Mutation	p.Ala797Thr(p.A797T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	134951807:134951807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560T>A
AA Mutation	p.Leu187His(p.L187H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135241217:135241217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416G>A
AA Mutation	p.Asp806Asn(p.D806N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135201561:135201561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218T>C
AA Mutation	p.Tyr740His(p.Y740H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135132894:135132894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>T
AA Mutation	p.Pro381Leu(p.P381L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135132842:135132842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373293977
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Trp(p.R364W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	134951773:134951773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781004053
CDS Mutation	c.526G>A
AA Mutation	p.Ala176Thr(p.A176T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135154175:135154175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321C>T
AA Mutation	p.His441Tyr(p.H441Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	134795654:134795654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23T>A
AA Mutation	p.Leu8Gln(p.L8Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135249409:135249409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373797543
CDS Mutation	c.2764G>A
AA Mutation	p.Ala922Thr(p.A922T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135162084:135162084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371083718
CDS Mutation	c.1489C>T
AA Mutation	p.Arg497Trp(p.R497W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135249454:135249454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2809T>C
AA Mutation	p.Phe937Leu(p.F937L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135106553:135106553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911G>T
AA Mutation	p.Arg304Leu(p.R304L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	134951492:134951492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245C>G
AA Mutation	p.Ala82Gly(p.A82G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135166024:135166024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642G>A
AA Mutation	p.Ala548Thr(p.A548T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	134951755:134951755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508C>T
AA Mutation	p.Arg170Trp(p.R170W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000398015
Start	135201487:135201487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2144A>T
AA Mutation	p.Gln715Leu(p.Q715L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398015
Start	135132913:135132913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367562212
CDS Mutation	c.1161G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398015
Start	135192778:135192778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2085C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398015
Start	134951721:134951721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398015
Start	135166023:135166023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776531462
CDS Mutation	c.1641G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398015
Start	135154162:135154162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1308C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398015
Start	135132841:135132841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398015
Start	134951486:134951486(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.244delG
AA Mutation	p.Ala82ProfsTer12(p.A82Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript