Mutation

Primary Site >> Stomach Cancer

Gene >> ERBB3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56099903:56099903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3003G>C
AA Mutation	p.Glu1001Asp(p.E1001D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000267101
Start	56088022:56088022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734C>T
AA Mutation	p.Ala245Val(p.A245V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56085070:56085070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Val104Met(p.V104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088585:56088585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917C>A
AA Mutation	p.Pro306His(p.P306H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56087887:56087887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706T>C
AA Mutation	p.Ser236Pro(p.S236P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56093820:56093820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1537G>T
AA Mutation	p.Gly513Cys(p.G513C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56095750:56095750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1999C>A
AA Mutation	p.Arg667Ser(p.R667S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56098868:56098868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193920754
CDS Mutation	c.2802G>C
AA Mutation	p.Gln934His(p.Q934H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56095709:56095709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958T>A
AA Mutation	p.Val653Glu(p.V653E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56098537:56098537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2654T>C
AA Mutation	p.Phe885Ser(p.F885S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56095751:56095751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000G>A
AA Mutation	p.Arg667His(p.R667H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56101241:56101241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3382G>A
AA Mutation	p.Gly1128Arg(p.G1128R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56085143:56085143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Ser128Asn(p.S128N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56095787:56095787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2036G>A
AA Mutation	p.Arg679Gln(p.R679Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56094445:56094445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748C>T
AA Mutation	p.Pro583Leu(p.P583L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56085115:56085115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759113437
CDS Mutation	c.355G>A
AA Mutation	p.Val119Ile(p.V119I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088823:56088823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064C>T
AA Mutation	p.Thr355Ile(p.T355I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56087876:56087876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695C>T
AA Mutation	p.Ala232Val(p.A232V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56093539:56093539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149951770
CDS Mutation	c.1469G>A
AA Mutation	p.Arg490His(p.R490H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088138:56088138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>A
AA Mutation	p.Gly284Arg(p.G284R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000267101
Start	56093346:56093346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375932235
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Trp(p.R426W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56101570:56101570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3544C>G
AA Mutation	p.Leu1182Val(p.L1182V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088609:56088609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941A>C
AA Mutation	p.Lys314Thr(p.K314T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56101266:56101266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758743468
CDS Mutation	c.3407G>A
AA Mutation	p.Arg1136His(p.R1136H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56095763:56095763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2012T>A
AA Mutation	p.Ile671Asn(p.I671N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088557:56088557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889G>T
AA Mutation	p.Asp297Tyr(p.D297Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56085070:56085070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>T
AA Mutation	p.Val104Leu(p.V104L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56087864:56087864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774589520
CDS Mutation	c.683A>G
AA Mutation	p.His228Arg(p.H228R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56101736:56101736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3710G>A
AA Mutation	p.Ser1237Asn(p.S1237N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56093362:56093362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1292T>C
AA Mutation	p.Leu431Ser(p.L431S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56087875:56087875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140656187
CDS Mutation	c.694G>A
AA Mutation	p.Ala232Thr(p.A232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56093401:56093401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777498890
CDS Mutation	c.1331G>A
AA Mutation	p.Arg444Gln(p.R444Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000267101
Start	56088748:56088748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989C>T
AA Mutation	p.Ala330Val(p.A330V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56101675:56101675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3649C>A
AA Mutation	p.Leu1217Ile(p.L1217I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088079:56088079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758573987
CDS Mutation	c.791T>C
AA Mutation	p.Val264Ala(p.V264A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56093428:56093428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144549266
CDS Mutation	c.1358G>A
AA Mutation	p.Arg453His(p.R453H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267101
Start	56083872:56083872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267101
Start	56088776:56088776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267101
Start	56099876:56099876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2976C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267101
Start	56097895:56097895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2571C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000267101
Start	56102036:56102037(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4012_4014dupAAT
AA Mutation	p.Asn1338dup(p.N1338dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript