Mutation

Primary Site >> Stomach Cancer

Gene >> ZC3H13

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45975499:45975499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528381815
CDS Mutation	c.2252G>A
AA Mutation	p.Arg751Gln(p.R751Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45985488:45985488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745791047
CDS Mutation	c.1529G>A
AA Mutation	p.Arg510His(p.R510H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45968762:45968762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375011338
CDS Mutation	c.3782G>A
AA Mutation	p.Arg1261Gln(p.R1261Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45969561:45969561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2983A>G
AA Mutation	p.Lys995Glu(p.K995E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45967974:45967974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3851G>A
AA Mutation	p.Arg1284Gln(p.R1284Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45969120:45969120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3424A>G
AA Mutation	p.Thr1142Ala(p.T1142A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45969834:45969834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2710C>T
AA Mutation	p.Arg904Cys(p.R904C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45985398:45985398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373662110
CDS Mutation	c.1619G>A
AA Mutation	p.Arg540His(p.R540H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	46042181:46042181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753807789
CDS Mutation	c.322T>C
AA Mutation	p.Ser108Pro(p.S108P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45985659:45985659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358G>A
AA Mutation	p.Arg453Gln(p.R453Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45988984:45988984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058G>T
AA Mutation	p.Arg353Ile(p.R353I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45975768:45975768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1983G>T
AA Mutation	p.Glu661Asp(p.E661D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45965369:45965369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4382A>G
AA Mutation	p.Tyr1461Cys(p.Y1461C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45979947:45979947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1778A>C
AA Mutation	p.His593Pro(p.H593P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45979966:45979966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1759A>G
AA Mutation	p.Ser587Gly(p.S587G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45969747:45969747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202084019
CDS Mutation	c.2797C>T
AA Mutation	p.Arg933Cys(p.R933C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45970409:45970409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144621814
CDS Mutation	c.2525G>A
AA Mutation	p.Arg842His(p.R842H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000242848
Start	45979951:45979951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1774T>G
AA Mutation	p.Tyr592Asp(p.Y592D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242848
Start	45967658:45967658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4167C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242848
Start	46011508:46011508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778630698
CDS Mutation	c.495A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242848
Start	45967553:45967553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4272G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242848
Start	45969964:45969964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2580A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242848
Start	45970366:45970366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2568T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	45969526:45969526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3018delA
AA Mutation	p.Lys1006AsnfsTer31(p.K1006Nfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	45963968:45963968(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4546delG
AA Mutation	p.Ala1516LeufsTer4(p.A1516Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	45969556:45969556(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2988delA
AA Mutation	p.Gly997AspfsTer40(p.G997Dfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	46003203:46003203(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.880delA
AA Mutation	p.Thr294GlnfsTer70(p.T294Qfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	46003246:46003246(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.837delA
AA Mutation	p.Lys279AsnfsTer8(p.K279Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	46011419:46011419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.584delA
AA Mutation	p.Lys195ArgfsTer18(p.K195Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000242848
Start	45975329:45975329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2422C>T
AA Mutation	p.Arg808Ter(p.R808*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000242848
Start	45985342:45985342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675C>T
AA Mutation	p.Arg559Ter(p.R559*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000242848
Start	45967798:45967798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4027C>T
AA Mutation	p.Arg1343Ter(p.R1343*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000242848
Start	46042196:46042196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Arg103Ter(p.R103*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000242848
Start	45967915:45967915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3910C>T
AA Mutation	p.Arg1304Ter(p.R1304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000242848
Start	45967867:45967867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3958C>T
AA Mutation	p.Gln1320Ter(p.Q1320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	45975467:45975468(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2282_2283dupAG
AA Mutation	p.Arg762SerfsTer104(p.R762Sfs*104)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	45969525:45969526(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3018dupA
AA Mutation	p.Arg1007ThrfsTer2(p.R1007Tfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242848
Start	46042201:46042202(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.301dupC
AA Mutation	p.Gln101ProfsTer13(p.Q101Pfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript