Mutation

Primary Site >> Stomach Cancer

Gene >> EPHA8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22596125:22596125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1717G>A
AA Mutation	p.Ala573Thr(p.A573T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000166244
Start	22576880:22576880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823G>C
AA Mutation	p.Ala275Pro(p.A275P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22600998:22600998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764652650
CDS Mutation	c.2639C>T
AA Mutation	p.Ala880Val(p.A880V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22593602:22593602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182997024
CDS Mutation	c.1519C>T
AA Mutation	p.Arg507Cys(p.R507C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22576713:22576713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656C>T
AA Mutation	p.Thr219Met(p.T219M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22586521:22586521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865C>A
AA Mutation	p.Leu289Met(p.L289M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22597411:22597411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1865C>T
AA Mutation	p.Ala622Val(p.A622V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22601323:22601323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141279306
CDS Mutation	c.2753G>A
AA Mutation	p.Arg918Gln(p.R918Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22598208:22598208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2174T>C
AA Mutation	p.Leu725Pro(p.L725P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22586615:22586615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765465256
CDS Mutation	c.959C>T
AA Mutation	p.Pro320Leu(p.P320L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22576461:22576461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404C>T
AA Mutation	p.Ala135Val(p.A135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22597756:22597756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2011G>T
AA Mutation	p.Ala671Ser(p.A671S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22588940:22588940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1049C>T
AA Mutation	p.Pro350Leu(p.P350L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22589134:22589134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539448650
CDS Mutation	c.1243G>A
AA Mutation	p.Val415Ile(p.V415I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22600770:22600770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2498C>T
AA Mutation	p.Ala833Val(p.A833V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22598954:22598954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2295C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22576345:22576345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22576531:22576531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22600786:22600786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2514C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22586553:22586553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372203085
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22597367:22597367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1821C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22576333:22576333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145476843
CDS Mutation	c.276C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000166244
Start	22588998:22588998(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1110delC
AA Mutation	p.Trp371GlyfsTer3(p.W371Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000166244
Start	22598934:22598934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2275C>T
AA Mutation	p.Arg759Ter(p.R759*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000166244
Start	22588930:22588930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1039G>T
AA Mutation	p.Glu347Ter(p.E347*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript