Mutation

Primary Site >> Stomach Cancer

Gene >> NBEA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35041106:35041106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.468A>C
AA Mutation	p.Glu156Asp(p.E156D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35566988:35566988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7006C>A
AA Mutation	p.Leu2336Ile(p.L2336I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35184005:35184005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4861A>G
AA Mutation	p.Ser1621Gly(p.S1621G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35070810:35070810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1529A>T
AA Mutation	p.Asp510Val(p.D510V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35472475:35472475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6524C>T
AA Mutation	p.Thr2175Met(p.T2175M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35142346:35142346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2414T>C
AA Mutation	p.Val805Ala(p.V805A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35070747:35070747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1466T>G
AA Mutation	p.Ile489Ser(p.I489S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35566976:35566976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6994T>G
AA Mutation	p.Leu2332Val(p.L2332V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35118462:35118462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2231G>T
AA Mutation	p.Arg744Ile(p.R744I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35628126:35628126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7495G>A
AA Mutation	p.Asp2499Asn(p.D2499N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35045033:35045033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613G>A
AA Mutation	p.Glu205Lys(p.E205K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35177075:35177075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4634G>A
AA Mutation	p.Arg1545His(p.R1545H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35628168:35628168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7537C>T
AA Mutation	p.Arg2513Cys(p.R2513C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35110930:35110930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1954T>C
AA Mutation	p.Trp652Arg(p.W652R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35041072:35041072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603808
CDS Mutation	c.434G>A
AA Mutation	p.Arg145Gln(p.R145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35550992:35550992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6766C>T
AA Mutation	p.Arg2256Trp(p.R2256W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35593400:35593400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116439886
CDS Mutation	c.7249G>A
AA Mutation	p.Val2417Ile(p.V2417I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35668474:35668474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8705G>A
AA Mutation	p.Gly2902Glu(p.G2902E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35195904:35195904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4968A>C
AA Mutation	p.Glu1656Asp(p.E1656D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35352197:35352197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6053A>G
AA Mutation	p.Glu2018Gly(p.E2018G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35655611:35655611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8161G>C
AA Mutation	p.Asp2721His(p.D2721H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35171354:35171354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4325T>C
AA Mutation	p.Val1442Ala(p.V1442A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35649781:35649781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7834A>G
AA Mutation	p.Ile2612Val(p.I2612V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35159078:35159078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2907G>T
AA Mutation	p.Glu969Asp(p.E969D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35670920:35670920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8770G>C
AA Mutation	p.Ala2924Pro(p.A2924P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35184026:35184026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4882G>A
AA Mutation	p.Ala1628Thr(p.A1628T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35309538:35309538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5849A>C
AA Mutation	p.Asn1950Thr(p.N1950T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35668392:35668392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8623C>A
AA Mutation	p.Gln2875Lys(p.Q2875K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35649673:35649673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7726C>A
AA Mutation	p.Pro2576Thr(p.P2576T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35655725:35655725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8275A>G
AA Mutation	p.Ile2759Val(p.I2759V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35195901:35195901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4965A>T
AA Mutation	p.Lys1655Asn(p.K1655N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35159940:35159940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3769G>A
AA Mutation	p.Ala1257Thr(p.A1257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35070755:35070755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1474G>T
AA Mutation	p.Ala492Ser(p.A492S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35159848:35159848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3677C>T
AA Mutation	p.Ala1226Val(p.A1226V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35196008:35196008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5072T>C
AA Mutation	p.Leu1691Ser(p.L1691S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35182478:35182478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4781G>T
AA Mutation	p.Ser1594Ile(p.S1594I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35566972:35566972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6990A>C
AA Mutation	p.Glu2330Asp(p.E2330D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35161820:35161820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3932C>G
AA Mutation	p.Pro1311Arg(p.P1311R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35058769:35058769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1145T>C
AA Mutation	p.Val382Ala(p.V382A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35164418:35164418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4142A>G
AA Mutation	p.Asn1381Ser(p.N1381S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35208749:35208749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5416A>G
AA Mutation	p.Thr1806Ala(p.T1806A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35550529:35550529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6638G>A
AA Mutation	p.Arg2213Gln(p.R2213Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35432336:35432336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200761216
CDS Mutation	c.6247C>T
AA Mutation	p.Arg2083Cys(p.R2083C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35159156:35159156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2985A>C
AA Mutation	p.Lys995Asn(p.K995N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	45
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35196064:35196064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561239166
CDS Mutation	c.5128G>A
AA Mutation	p.Glu1710Lys(p.E1710K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	46
Mutation Consequence	missense_variant
Transcription ID	ENST00000400445
Start	35349122:35349122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5918C>T
AA Mutation	p.Ala1973Val(p.A1973V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	35432356:35432356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6267T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	35159714:35159714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3543T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	35208754:35208754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5421T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	35157228:35157228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2802C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	35667471:35667471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770305071
CDS Mutation	c.8499C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	35118394:35118394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2163T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	35069991:35069991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	35550985:35550985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6759C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	55
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400445
Start	34943111:34943111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764089764
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400445
Start	35157090:35157093(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2664_2667delGTGT
AA Mutation	p.Gln888HisfsTer40(p.Q888Hfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	57
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400445
Start	35164406:35164406(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4134delT
AA Mutation	p.Phe1378LeufsTer13(p.F1378Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	58
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400445
Start	35159526:35159526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763376147
CDS Mutation	c.3362delA
AA Mutation	p.Asn1121MetfsTer9(p.N1121Mfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	59
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400445
Start	35550967:35550967(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6747delA
AA Mutation	p.Val2250LeufsTer10(p.V2250Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	60
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400445
Start	35649727:35649727(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7781delC
AA Mutation	p.Pro2594LeufsTer6(p.P2594Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	61
Mutation Consequence	stop_gained
Transcription ID	ENST00000400445
Start	35667505:35667505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8533C>T
AA Mutation	p.Arg2845Ter(p.R2845*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	62
Mutation Consequence	stop_gained
Transcription ID	ENST00000400445
Start	35159100:35159100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2929A>T
AA Mutation	p.Lys977Ter(p.K977*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	63
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400445
Start	35159525:35159526(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3362dupA
AA Mutation	p.Asn1121LysfsTer2(p.N1121Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	64
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400445
Start	35157226:35157227(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2800_2801insAAAAAAATTT
AA Mutation	p.Gly934GlufsTer22(p.G934Efs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	65
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400445
Start	35550966:35550967(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.6747dupA
AA Mutation	p.Val2250SerfsTer4(p.V2250Sfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	66
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000400445
Start	35606425:35606425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7297-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript