Mutation

Primary Site >> Stomach Cancer

Gene >> EPHA5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65602159:65602159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392A>C
AA Mutation	p.Lys131Thr(p.K131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65366053:65366053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1929A>C
AA Mutation	p.Lys643Asn(p.K643N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65601719:65601719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749830045
CDS Mutation	c.832G>A
AA Mutation	p.Ala278Thr(p.A278T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65602156:65602156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395T>G
AA Mutation	p.Phe132Cys(p.F132C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65324131:65324131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139793674
CDS Mutation	c.3097G>A
AA Mutation	p.Gly1033Arg(p.G1033R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65336105:65336105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2679A>C
AA Mutation	p.Glu893Asp(p.E893D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65377037:65377037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1817C>T
AA Mutation	p.Ala606Val(p.A606V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65365080:65365080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173G>A
AA Mutation	p.Ala725Thr(p.A725T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65365140:65365140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2113G>T
AA Mutation	p.Ala705Ser(p.A705S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65602005:65602005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546C>A
AA Mutation	p.Ser182Arg(p.S182R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65669633:65669633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110G>A
AA Mutation	p.Arg37Gln(p.R37Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65669571:65669571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172A>C
AA Mutation	p.Ser58Arg(p.S58R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65324175:65324175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3053A>T
AA Mutation	p.Lys1018Met(p.K1018M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65367419:65367419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1862G>A
AA Mutation	p.Cys621Tyr(p.C621Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65601872:65601872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746706656
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Cys(p.R227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65420473:65420473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1495A>G
AA Mutation	p.Ile499Val(p.I499V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65669600:65669600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143C>T
AA Mutation	p.Ala48Val(p.A48V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65495431:65495431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1023T>A
AA Mutation	p.Asp341Glu(p.D341E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65420542:65420542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426A>G
AA Mutation	p.Lys476Glu(p.K476E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65495495:65495495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959G>A
AA Mutation	p.Gly320Asp(p.G320D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65367390:65367390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1891G>A
AA Mutation	p.Glu631Lys(p.E631K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65351505:65351505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2392C>A
AA Mutation	p.His798Asn(p.H798N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65602157:65602157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394T>C
AA Mutation	p.Phe132Leu(p.F132L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65331997:65331997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2984A>C
AA Mutation	p.Asp995Ala(p.D995A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65332016:65332016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2965A>C
AA Mutation	p.Asn989His(p.N989H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000273854
Start	65324209:65324209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777838691
CDS Mutation	c.3019C>T
AA Mutation	p.Arg1007Trp(p.R1007W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65332107:65332107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771745177
CDS Mutation	c.2874A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65490582:65490582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1197C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65601795:65601795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65420540:65420540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1428A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65404463:65404463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768844742
CDS Mutation	c.1701C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65669607:65669607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65601747:65601747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373719926
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65490660:65490660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1119C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65414291:65414291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1680C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65601852:65601852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747700048
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65490431:65490431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273854
Start	65490522:65490522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753971619
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273854
Start	65602210:65602210(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.341delT
AA Mutation	p.Leu114Ter(p.L114*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273854
Start	65643367:65643367(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.242delA
AA Mutation	p.Asn81MetfsTer24(p.N81Mfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273854
Start	65601855:65601855(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.696delA
AA Mutation	p.Lys232AsnfsTer36(p.K232Nfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273854
Start	65351594:65351594(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2303delA
AA Mutation	p.Asn768ThrfsTer7(p.N768Tfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273854
Start	65601928:65601928(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.623delA
AA Mutation	p.Lys208ArgfsTer60(p.K208Rfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273854
Start	65490705:65490705(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1074delC
AA Mutation	p.Ser359LeufsTer63(p.S359Lfs*63)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	45
Mutation Consequence	stop_gained
Transcription ID	ENST00000273854
Start	65367390:65367390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1891G>T
AA Mutation	p.Glu631Ter(p.E631*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	46
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273854
Start	65490562:65490563(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1215_1216dupTG
AA Mutation	p.Glu406ValfsTer17(p.E406Vfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273854
Start	65420536:65420537(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1431dupA
AA Mutation	p.Gly478ArgfsTer26(p.G478Rfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript