Mutation

Primary Site >> Stomach Cancer

Gene >> NAV1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201718691:201718691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162G>A
AA Mutation	p.Gly388Ser(p.G388S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201803689:201803689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775861896
CDS Mutation	c.3614C>T
AA Mutation	p.Ala1205Val(p.A1205V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201649081:201649081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413C>T
AA Mutation	p.Thr138Met(p.T138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201781283:201781283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1637C>T
AA Mutation	p.Thr546Ile(p.T546I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201649200:201649200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532C>T
AA Mutation	p.Pro178Ser(p.P178S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367296
Start	201809535:201809535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4399A>G
AA Mutation	p.Lys1467Glu(p.K1467E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201718433:201718433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146415554
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Cys(p.R302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201782712:201782712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2200A>T
AA Mutation	p.Thr734Ser(p.T734S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201810024:201810024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4480G>A
AA Mutation	p.Val1494Met(p.V1494M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201810703:201810703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369328574
CDS Mutation	c.4742G>A
AA Mutation	p.Arg1581His(p.R1581H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201649219:201649219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551C>T
AA Mutation	p.Pro184Leu(p.P184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201817152:201817152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5405C>T
AA Mutation	p.Pro1802Leu(p.P1802L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201812581:201812581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5141G>A
AA Mutation	p.Arg1714Gln(p.R1714Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201790747:201790747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3302C>T
AA Mutation	p.Thr1101Met(p.T1101M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201712894:201712894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835C>A
AA Mutation	p.Leu279Met(p.L279M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201811645:201811645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769287371
CDS Mutation	c.4840C>T
AA Mutation	p.Arg1614Trp(p.R1614W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201648850:201648850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182C>T
AA Mutation	p.Ala61Val(p.A61V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201782475:201782475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963G>A
AA Mutation	p.Ala655Thr(p.A655T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201648877:201648877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.209G>T
AA Mutation	p.Gly70Val(p.G70V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000367296
Start	201782239:201782239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759712759
CDS Mutation	c.1727G>A
AA Mutation	p.Arg576His(p.R576H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201812588:201812588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770006935
CDS Mutation	c.5148C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201718516:201718516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201810629:201810629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4668C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201782315:201782315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1803T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201788583:201788583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751797090
CDS Mutation	c.3111C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201781104:201781104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749363564
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201783583:201783583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144457633
CDS Mutation	c.2535G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201648896:201648896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.228C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201718576:201718576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770408542
CDS Mutation	c.1047C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201782306:201782306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367296
Start	201782522:201782522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751158000
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367296
Start	201649144:201649144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.481delC
AA Mutation	p.Leu161TrpfsTer33(p.L161Wfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367296
Start	201819914:201819914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5617delC
AA Mutation	p.Leu1873PhefsTer66(p.L1873Ffs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367296
Start	201803700:201803700(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3632delA
AA Mutation	p.Lys1211ArgfsTer17(p.K1211Rfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367296
Start	201807985:201807985(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3686delA
AA Mutation	p.Lys1229ArgfsTer12(p.K1229Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367296
Start	201781090:201781090(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1449delA
AA Mutation	p.Lys483AsnfsTer9(p.K483Nfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367296
Start	201649143:201649144(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.481dupC
AA Mutation	p.Leu161ProfsTer30(p.L161Pfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript