Mutation

Primary Site >> Stomach Cancer

Gene >> EPHA3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89210326:89210326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620A>T
AA Mutation	p.Lys207Met(p.K207M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89210326:89210326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620A>C
AA Mutation	p.Lys207Thr(p.K207T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89419241:89419241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925T>G
AA Mutation	p.Leu642Arg(p.L642R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89395893:89395893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363T>G
AA Mutation	p.Leu455Val(p.L455V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89210277:89210277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571G>T
AA Mutation	p.Ala191Ser(p.A191S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89341806:89341806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022T>C
AA Mutation	p.Val341Ala(p.V341A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89408099:89408099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1730A>T
AA Mutation	p.Asp577Val(p.D577V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89210269:89210269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563C>T
AA Mutation	p.Ala188Val(p.A188V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89341907:89341907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123C>T
AA Mutation	p.Pro375Ser(p.P375S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89431295:89431295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2282A>T
AA Mutation	p.Lys761Met(p.K761M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89479446:89479446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2896A>G
AA Mutation	p.Ile966Val(p.I966V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89419284:89419284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1968A>C
AA Mutation	p.Lys656Asn(p.K656N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89209905:89209905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199A>G
AA Mutation	p.Thr67Ala(p.T67A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89127218:89127218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98T>G
AA Mutation	p.Leu33Arg(p.L33R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89450255:89450255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2575G>A
AA Mutation	p.Asp859Asn(p.D859N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89479404:89479404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2854A>G
AA Mutation	p.Lys952Glu(p.K952E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89407361:89407361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1687T>G
AA Mutation	p.Leu563Val(p.L563V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89419273:89419273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1957A>G
AA Mutation	p.Lys653Glu(p.K653E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89472547:89472547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2774C>T
AA Mutation	p.Thr925Ile(p.T925I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89413252:89413252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874A>C
AA Mutation	p.Lys625Thr(p.K625T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89341879:89341879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095A>C
AA Mutation	p.Lys365Asn(p.K365N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89450210:89450210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2530C>T
AA Mutation	p.Pro844Ser(p.P844S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89407309:89407309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200724434
CDS Mutation	c.1635C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89472518:89472518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2745A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89210159:89210159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89449284:89449284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372376671
CDS Mutation	c.2406G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89419260:89419260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138119313
CDS Mutation	c.1944T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89472521:89472521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2748A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89127258:89127258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89342020:89342020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1236T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89210450:89210450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150099876
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336596
Start	89210304:89210304(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.602delA
AA Mutation	p.Lys201SerfsTer6(p.K201Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336596
Start	89450213:89450213(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2538delC
AA Mutation	p.Met847TrpfsTer10(p.M847Wfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336596
Start	89419248:89419248(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1938delA
AA Mutation	p.Glu647ArgfsTer9(p.E647Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336596
Start	89341874:89341874(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1095delA
AA Mutation	p.Lys365AsnfsTer6(p.K365Nfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000336596
Start	89341937:89341937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153C>T
AA Mutation	p.Arg385Ter(p.R385*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	splice_donor_variant;intron_variant
Transcription ID	ENST00000336596
Start	89449375:89449378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2496+4_2496+7delAGTA
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	38
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000336596
Start	89450175:89450175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2497-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript