Mutation

Primary Site >> Stomach Cancer

Gene >> EPHA2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16137891:16137891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754988701
CDS Mutation	c.1274G>A
AA Mutation	p.Arg425His(p.R425H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16133302:16133302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1931C>T
AA Mutation	p.Ala644Val(p.A644V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16135161:16135161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457G>A
AA Mutation	p.Arg486His(p.R486H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16133540:16133540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1805T>C
AA Mutation	p.Leu602Ser(p.L602S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358432
Start	16129435:16129435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2824G>A
AA Mutation	p.Asp942Asn(p.D942N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16135691:16135691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1392C>A
AA Mutation	p.Ser464Arg(p.S464R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16132161:16132161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2228G>A
AA Mutation	p.Arg743His(p.R743H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16137913:16137913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568736295
CDS Mutation	c.1252G>A
AA Mutation	p.Val418Ile(p.V418I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16130389:16130389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2506C>T
AA Mutation	p.Leu836Phe(p.L836F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16131785:16131785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2411G>A
AA Mutation	p.Gly804Asp(p.G804D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16132177:16132177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2212C>A
AA Mutation	p.Arg738Ser(p.R738S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16132183:16132183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2206G>C
AA Mutation	p.Val736Leu(p.V736L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16133522:16133522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1823T>G
AA Mutation	p.Ile608Ser(p.I608S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16132116:16132116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2273T>G
AA Mutation	p.Phe758Cys(p.F758C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16131822:16131822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55869078
CDS Mutation	c.2374C>T
AA Mutation	p.Arg792Trp(p.R792W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16138075:16138075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150248625
CDS Mutation	c.1090G>A
AA Mutation	p.Val364Ile(p.V364I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16133192:16133192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140398645
CDS Mutation	c.2041G>A
AA Mutation	p.Val681Ile(p.V681I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16148698:16148698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756877965
CDS Mutation	c.503G>A
AA Mutation	p.Arg168His(p.R168H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16135099:16135099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1519G>A
AA Mutation	p.Val507Met(p.V507M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16138411:16138411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843T>A
AA Mutation	p.Phe281Leu(p.F281L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16133307:16133307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759675163
CDS Mutation	c.1926G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16135133:16135133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768864167
CDS Mutation	c.1485C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16132112:16132112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2277C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16138037:16138037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779516824
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16129517:16129517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749092028
CDS Mutation	c.2742G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16135704:16135704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1379delC
AA Mutation	p.Pro460ArgfsTer33(p.P460Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16134483:16134483(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1667delT
AA Mutation	p.Phe556SerfsTer27(p.F556Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16148482:16148482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.719delG
AA Mutation	p.Gly240ValfsTer153(p.G240Vfs*153)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16148638:16148638(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.563delG
AA Mutation	p.Cys188LeufsTer205(p.C188Lfs*205)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16148688:16148688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.513delG
AA Mutation	p.Pro172ArgfsTer221(p.P172Rfs*221)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16133553:16133554(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1791dupC
AA Mutation	p.Asn598GlnfsTer96(p.N598Qfs*96)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript