Mutation

Primary Site >> Stomach Cancer

Gene >> ERBB4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211561997:211561997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393T>C
AA Mutation	p.Leu798Pro(p.L798P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211387064:211387064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3270A>C
AA Mutation	p.Glu1090Asp(p.E1090D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211384054:211384054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768312275
CDS Mutation	c.3488T>C
AA Mutation	p.Leu1163Pro(p.L1163P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211383874:211383874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3668A>T
AA Mutation	p.Lys1223Met(p.K1223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211562070:211562070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2320A>G
AA Mutation	p.Ser774Gly(p.S774G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211713626:211713626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.906T>G
AA Mutation	p.Ser302Arg(p.S302R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211561997:211561997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2393T>A
AA Mutation	p.Leu798His(p.L798H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211424241:211424241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397514262
CDS Mutation	c.2780G>A
AA Mutation	p.Arg927Gln(p.R927Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211383722:211383722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3820A>T
AA Mutation	p.Ile1274Phe(p.I1274F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211701994:211701994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462C>T
AA Mutation	p.Arg488Trp(p.R488W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211788125:211788125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456C>G
AA Mutation	p.Asn152Lys(p.N152K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211386981:211386981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3353A>G
AA Mutation	p.His1118Arg(p.H1118R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211422035:211422035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763644012
CDS Mutation	c.2936G>A
AA Mutation	p.Arg979Gln(p.R979Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211947535:211947535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751175543
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Cys(p.R106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	212124838:212124838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372631205
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Cys(p.R50C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211619248:211619248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2230G>T
AA Mutation	p.Val744Leu(p.V744L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211725185:211725185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771486473
CDS Mutation	c.632C>T
AA Mutation	p.Thr211Met(p.T211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211947592:211947592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143662416
CDS Mutation	c.259G>A
AA Mutation	p.Val87Met(p.V87M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211705355:211705355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1161G>T
AA Mutation	p.Glu387Asp(p.E387D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211387029:211387029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3305T>G
AA Mutation	p.Phe1102Cys(p.F1102C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	212124861:212124861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125T>C
AA Mutation	p.Leu42Pro(p.L42P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211623995:211623995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2129T>G
AA Mutation	p.Leu710Arg(p.L710R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211679109:211679109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761773013
CDS Mutation	c.1565C>T
AA Mutation	p.Ser522Leu(p.S522L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211424197:211424197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2824C>T
AA Mutation	p.Pro942Ser(p.P942S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211561997:211561997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393T>G
AA Mutation	p.Leu798Arg(p.L798R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211387147:211387147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3187C>A
AA Mutation	p.Gln1063Lys(p.Q1063K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211383883:211383883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3659A>C
AA Mutation	p.Glu1220Ala(p.E1220A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211701975:211701975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1481A>G
AA Mutation	p.Glu494Gly(p.E494G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211712100:211712100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074C>A
AA Mutation	p.Asn358Lys(p.N358K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211561929:211561929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2461C>A
AA Mutation	p.Leu821Ile(p.L821I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211725099:211725099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718G>A
AA Mutation	p.Gly240Arg(p.G240R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211657823:211657823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1877A>C
AA Mutation	p.Asn626Thr(p.N626T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211383871:211383871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3671A>C
AA Mutation	p.Asn1224Thr(p.N1224T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211420571:211420571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3005A>C
AA Mutation	p.Lys1002Thr(p.K1002T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211431070:211431070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369248674
CDS Mutation	c.2518G>A
AA Mutation	p.Val840Ile(p.V840I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211947534:211947534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>A
AA Mutation	p.Arg106His(p.R106H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211713552:211713552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980C>T
AA Mutation	p.Thr327Ile(p.T327I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211424293:211424293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754195521
CDS Mutation	c.2728A>G
AA Mutation	p.Ile910Val(p.I910V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211704191:211704191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202T>C
AA Mutation	p.Phe401Ser(p.F401S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211947561:211947561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290T>C
AA Mutation	p.Leu97Pro(p.L97P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211386940:211386940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3394C>T
AA Mutation	p.Pro1132Ser(p.P1132S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211386885:211386885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3449A>G
AA Mutation	p.Tyr1150Cys(p.Y1150C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211420571:211420571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751857242
CDS Mutation	c.3005A>G
AA Mutation	p.Lys1002Arg(p.K1002R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211383874:211383874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3668A>C
AA Mutation	p.Lys1223Thr(p.K1223T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	45
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	212538520:212538520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748663394
CDS Mutation	c.11C>A
AA Mutation	p.Ala4Glu(p.A4E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	46
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211750675:211750675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769311799
CDS Mutation	c.586C>T
AA Mutation	p.Arg196Cys(p.R196C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	47
Mutation Consequence	missense_variant
Transcription ID	ENST00000342788
Start	211725168:211725168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649T>C
AA Mutation	p.Cys217Arg(p.C217R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342788
Start	211387954:211387954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3174C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342788
Start	211387064:211387064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3270A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342788
Start	211387028:211387028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3306T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342788
Start	211665343:211665343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1851C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342788
Start	211788134:211788134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342788
Start	211422061:211422061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2910G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342788
Start	211679108:211679108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774467771
CDS Mutation	c.1566G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	55
Mutation Consequence	frameshift_variant;start_lost
Transcription ID	ENST00000342788
Start	212538530:212538530(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1delA
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342788
Start	211705386:211705386(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1130delC
AA Mutation	p.Pro377LeufsTer8(p.P377Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	57
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342788
Start	211384012:211384012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3530delA
AA Mutation	p.Asn1177MetfsTer27(p.N1177Mfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	58
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000342788
Start	211424155:211424156(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2865dupA
AA Mutation	p.Cys956MetfsTer5(p.C956Mfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	59
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000342788
Start	211428485:211428485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2644-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript