Mutation

Primary Site >> Stomach Cancer

Gene >> ICE1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5461843:5461843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2509C>T
AA Mutation	p.Leu837Phe(p.L837F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5466415:5466415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763288159
CDS Mutation	c.5974G>A
AA Mutation	p.Ala1992Thr(p.A1992T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5476022:5476022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6463C>A
AA Mutation	p.His2155Asn(p.H2155N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5457406:5457406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766C>A
AA Mutation	p.Pro256Thr(p.P256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5464502:5464502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5168A>G
AA Mutation	p.His1723Arg(p.H1723R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5476035:5476035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375797140
CDS Mutation	c.6476C>T
AA Mutation	p.Ala2159Val(p.A2159V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5436466:5436466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133A>G
AA Mutation	p.Ile45Val(p.I45V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5462615:5462615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3281T>C
AA Mutation	p.Leu1094Ser(p.L1094S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5461037:5461037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1703G>A
AA Mutation	p.Arg568Gln(p.R568Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5461718:5461718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2384A>G
AA Mutation	p.Asp795Gly(p.D795G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5462103:5462103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2769C>G
AA Mutation	p.Ser923Arg(p.S923R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5464351:5464351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202035188
CDS Mutation	c.5017C>T
AA Mutation	p.Arg1673Cys(p.R1673C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5463174:5463174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3840A>T
AA Mutation	p.Lys1280Asn(p.K1280N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5463962:5463962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4628A>G
AA Mutation	p.Asn1543Ser(p.N1543S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5468834:5468834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6068C>T
AA Mutation	p.Pro2023Leu(p.P2023L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5463905:5463905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4571A>C
AA Mutation	p.Gln1524Pro(p.Q1524P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5457483:5457483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843T>G
AA Mutation	p.Asn281Lys(p.N281K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5463257:5463257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148095940
CDS Mutation	c.3923C>T
AA Mutation	p.Thr1308Met(p.T1308M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5462313:5462313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2979C>A
AA Mutation	p.Asp993Glu(p.D993E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5461544:5461544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2210C>T
AA Mutation	p.Ser737Leu(p.S737L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5464625:5464625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5291G>A
AA Mutation	p.Arg1764Gln(p.R1764Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5473562:5473562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6227C>T
AA Mutation	p.Ala2076Val(p.A2076V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5463403:5463403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4069G>T
AA Mutation	p.Asp1357Tyr(p.D1357Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000296564
Start	5464487:5464487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5153C>T
AA Mutation	p.Ala1718Val(p.A1718V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5461644:5461644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2310A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5462694:5462694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376280358
CDS Mutation	c.3360C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5468931:5468931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6165G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5464624:5464624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5290C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5466414:5466414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532424447
CDS Mutation	c.5973C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5462793:5462793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544295645
CDS Mutation	c.3459G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5462349:5462349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3015C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5461083:5461083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1749C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296564
Start	5461338:5461338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779231382
CDS Mutation	c.2004G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296564
Start	5457612:5457612(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.978delT
AA Mutation	p.Phe326LeufsTer82(p.F326Lfs*82)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296564
Start	5464103:5464103(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4773delA
AA Mutation	p.Ala1592LeufsTer14(p.A1592Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296564
Start	5460686:5460686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1353delA
AA Mutation	p.Glu451AspfsTer8(p.E451Dfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296564
Start	5463069:5463069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3740delA
AA Mutation	p.Asn1247IlefsTer17(p.N1247Ifs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296564
Start	5462640:5462640(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3311delG
AA Mutation	p.Gly1104GlufsTer6(p.G1104Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000296564
Start	5460850:5460850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516C>T
AA Mutation	p.Arg506Ter(p.R506*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000296564
Start	5476003:5476003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6444G>A
AA Mutation	p.Trp2148Ter(p.W2148*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296564
Start	5461117:5461118(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1788dupA
AA Mutation	p.Glu597ArgfsTer13(p.E597Rfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript