Mutation

Primary Site >> Stomach Cancer

Gene >> EP300

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41117712:41117712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620A>G
AA Mutation	p.Tyr207Cys(p.Y207C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41127689:41127689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109G>A
AA Mutation	p.Arg370His(p.R370H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41176920:41176920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5209C>T
AA Mutation	p.Arg1737Cys(p.R1737C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41176346:41176346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4879C>T
AA Mutation	p.Arg1627Trp(p.R1627W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41177759:41177759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6048G>A
AA Mutation	p.Met2016Ile(p.M2016I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41131547:41131547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533244094
CDS Mutation	c.1442C>T
AA Mutation	p.Pro481Leu(p.P481L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41178561:41178561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6850A>G
AA Mutation	p.Met2284Val(p.M2284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41178813:41178813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7102G>A
AA Mutation	p.Asp2368Asn(p.D2368N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41170516:41170516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4397G>T
AA Mutation	p.Trp1466Leu(p.W1466L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41176969:41176969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5258G>T
AA Mutation	p.Cys1753Phe(p.C1753F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41168762:41168762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4067G>A
AA Mutation	p.Arg1356Gln(p.R1356Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41178124:41178124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587778258
CDS Mutation	c.6413C>T
AA Mutation	p.Ala2138Val(p.A2138V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41177002:41177002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5291T>G
AA Mutation	p.Val1764Gly(p.V1764G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41170507:41170507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4388T>G
AA Mutation	p.Leu1463Arg(p.L1463R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41178591:41178591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6880C>A
AA Mutation	p.Leu2294Ile(p.L2294I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41127562:41127562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.982C>T
AA Mutation	p.His328Tyr(p.H328Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41177170:41177170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5459A>G
AA Mutation	p.His1820Arg(p.H1820R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41137769:41137769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1739G>A
AA Mutation	p.Arg580Gln(p.R580Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41093024:41093024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20A>G
AA Mutation	p.Glu7Gly(p.E7G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000263253
Start	41178327:41178327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6616G>T
AA Mutation	p.Ala2206Ser(p.A2206S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263253
Start	41178281:41178281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772427602
CDS Mutation	c.6570A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263253
Start	41177525:41177525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112948044
CDS Mutation	c.5814G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263253
Start	41177801:41177801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749621134
CDS Mutation	c.6090A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263253
Start	41117536:41117536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376779611
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263253
Start	41177300:41177300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5589A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263253
Start	41178431:41178431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753617318
CDS Mutation	c.6720A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000263253
Start	41152347:41152348(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3139_3140insCGTAAGAATTTTTAGTATTCC
AA Mutation	p.Lys1047delinsThrTerGluPheLeuValPheGln(p.K1047delinsT*EFLVFQ)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263253
Start	41149777:41149778(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2398dupT
AA Mutation	p.Ser800PhefsTer38(p.S800Ffs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263253
Start	41173751:41173752(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4749dupA
AA Mutation	p.Leu1584ThrfsTer9(p.L1584Tfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000263253
Start	41160641:41160641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3591-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	31
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000263253
Start	41172497:41172497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4453-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	32
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263253
Start	41131635:41131635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript