Mutation

Primary Site >> Stomach Cancer

Gene >> EPHA4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221426125:221426125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2864G>A
AA Mutation	p.Gly955Asp(p.G955D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221563986:221563986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568G>A
AA Mutation	p.Ala190Thr(p.A190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221426071:221426071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140023331
CDS Mutation	c.2918G>A
AA Mutation	p.Arg973Gln(p.R973Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221564178:221564178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376T>C
AA Mutation	p.Tyr126His(p.Y126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221426516:221426516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2794T>G
AA Mutation	p.Phe932Val(p.F932V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221446177:221446177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1720A>G
AA Mutation	p.Ser574Gly(p.S574G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221443529:221443529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765720231
CDS Mutation	c.1852G>A
AA Mutation	p.Ala618Thr(p.A618T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221564238:221564238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316A>T
AA Mutation	p.Arg106Trp(p.R106W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221563808:221563808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746C>T
AA Mutation	p.Ala249Val(p.A249V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221563809:221563809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745G>A
AA Mutation	p.Ala249Thr(p.A249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221455575:221455575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1687C>T
AA Mutation	p.Leu563Phe(p.L563F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221456767:221456767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1449G>C
AA Mutation	p.Gln483His(p.Q483H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221563790:221563790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764T>C
AA Mutation	p.Val255Ala(p.V255A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221434153:221434153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2485T>C
AA Mutation	p.Ser829Pro(p.S829P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000281821
Start	221436529:221436529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2216A>T
AA Mutation	p.Asp739Val(p.D739V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281821
Start	221442842:221442842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749760114
CDS Mutation	c.2061C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281821
Start	221501033:221501033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281821
Start	221434262:221434262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141789136
CDS Mutation	c.2376G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281821
Start	221429969:221429969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371830529
CDS Mutation	c.2679G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281821
Start	221436513:221436513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2232T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221568759:221568759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771415392
CDS Mutation	c.118C>T
AA Mutation	p.Gln40Ter(p.Q40*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221564301:221564301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253C>T
AA Mutation	p.Arg85Ter(p.R85*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221443553:221443553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828C>T
AA Mutation	p.Arg610Ter(p.R610*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221568753:221568753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>T
AA Mutation	p.Glu42Ter(p.E42*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000281821
Start	221564283:221564283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Ter(p.R91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281821
Start	221457900:221457901(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1408dupG
AA Mutation	p.Val470GlyfsTer6(p.V470Gfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000281821
Start	221457864:221457864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1443+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	28
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000281821
Start	221564034:221564084(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.470_520delTGGACATTGGTGACAGAATCATGAAGCTGAACACCGAGATCCGGGATGTAG
AA Mutation	p.Val157_Val173del(p.V157_V173del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript