Mutation

Primary Site >> Stomach Cancer

Gene >> HIVEP3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41583996:41583996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802A>G
AA Mutation	p.Ile268Val(p.I268V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41582355:41582355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2443C>T
AA Mutation	p.Pro815Ser(p.P815S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41583354:41583354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444G>A
AA Mutation	p.Asp482Asn(p.D482N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41583044:41583044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751390922
CDS Mutation	c.1754G>A
AA Mutation	p.Arg585Gln(p.R585Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41579759:41579759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5039C>T
AA Mutation	p.Ser1680Phe(p.S1680F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41584567:41584567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231G>T
AA Mutation	p.Gln77His(p.Q77H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41513055:41513055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6166G>A
AA Mutation	p.Glu2056Lys(p.E2056K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41581700:41581700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766672681
CDS Mutation	c.3098C>T
AA Mutation	p.Ala1033Val(p.A1033V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41513727:41513727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5494G>T
AA Mutation	p.Asp1832Tyr(p.D1832Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41583709:41583709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089G>T
AA Mutation	p.Lys363Asn(p.K363N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41582297:41582297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2501C>T
AA Mutation	p.Ala834Val(p.A834V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41584481:41584481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149979631
CDS Mutation	c.317C>T
AA Mutation	p.Ser106Leu(p.S106L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41583125:41583125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143274774
CDS Mutation	c.1673G>A
AA Mutation	p.Arg558Gln(p.R558Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41513288:41513288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144265546
CDS Mutation	c.5933G>A
AA Mutation	p.Arg1978His(p.R1978H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41584745:41584745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199627359
CDS Mutation	c.53G>A
AA Mutation	p.Arg18Gln(p.R18Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41582045:41582045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2753G>A
AA Mutation	p.Gly918Glu(p.G918E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41582829:41582829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1969A>G
AA Mutation	p.Asn657Asp(p.N657D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41582840:41582840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1958A>C
AA Mutation	p.Lys653Thr(p.K653T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41583281:41583281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753023139
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506Gln(p.R506Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41584022:41584022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776A>G
AA Mutation	p.Tyr259Cys(p.Y259C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41524807:41524807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5311A>G
AA Mutation	p.Lys1771Glu(p.K1771E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41583425:41583425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458Gln(p.R458Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41512993:41512993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6228G>T
AA Mutation	p.Gln2076His(p.Q2076H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41575613:41575613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5138G>T
AA Mutation	p.Gly1713Val(p.G1713V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41580300:41580300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4498T>C
AA Mutation	p.Ser1500Pro(p.S1500P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41581773:41581773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746529841
CDS Mutation	c.3025C>T
AA Mutation	p.Arg1009Cys(p.R1009C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000247584
Start	41513699:41513699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760265220
CDS Mutation	c.5522C>A
AA Mutation	p.Ala1841Asp(p.A1841D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41579794:41579794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765704017
CDS Mutation	c.5004G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41581507:41581507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3291A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41513047:41513047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6174C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41580499:41580499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4299A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41510457:41510457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374547284
CDS Mutation	c.7215C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41583721:41583721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201110520
CDS Mutation	c.1077G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41575567:41575567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781357885
CDS Mutation	c.5184G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41580097:41580097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4701T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41584132:41584132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756968051
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41524813:41524813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5305C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41580562:41580562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4236A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41581504:41581504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537713789
CDS Mutation	c.3294C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41582755:41582755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2043A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41579758:41579758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748776038
CDS Mutation	c.5040C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247584
Start	41581255:41581255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3543T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247584
Start	41583138:41583138(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1660delC
AA Mutation	p.His554ThrfsTer20(p.H554Tfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247584
Start	41584450:41584450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.348delG
AA Mutation	p.Ser117ProfsTer9(p.S117Pfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247584
Start	41583197:41583197(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1601delC
AA Mutation	p.Pro534LeufsTer5(p.P534Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	46
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247584
Start	41513573:41513573(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5648delC
AA Mutation	p.Pro1883ArgfsTer42(p.P1883Rfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247584
Start	41583045:41583045(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1753delC
AA Mutation	p.Arg585GlyfsTer3(p.R585Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	48
Mutation Consequence	stop_gained
Transcription ID	ENST00000247584
Start	41581317:41581317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3481G>T
AA Mutation	p.Glu1161Ter(p.E1161*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	49
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247584
Start	41524838:41524839(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5279dupG
AA Mutation	p.Ile1761AsnfsTer18(p.I1761Nfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247584
Start	41580452:41580453(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4345dupA
AA Mutation	p.Arg1449LysfsTer12(p.R1449Kfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript