Mutation

Primary Site >> Stomach Cancer

Gene >> ERBB2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39707032:39707032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116C>T
AA Mutation	p.Pro39Leu(p.P39L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39724745:39724745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144434331
CDS Mutation	c.2327G>T
AA Mutation	p.Gly776Val(p.G776V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39723348:39723348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1976T>A
AA Mutation	p.Val659Asp(p.V659D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39725139:39725139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2584A>G
AA Mutation	p.Thr862Ala(p.T862A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39726959:39726959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566053951
CDS Mutation	c.3115G>A
AA Mutation	p.Ala1039Thr(p.A1039T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39723405:39723405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2033G>A
AA Mutation	p.Arg678Gln(p.R678Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39711955:39711955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>T
AA Mutation	p.Ser310Phe(p.S310F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39726610:39726610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2921C>T
AA Mutation	p.Ser974Phe(p.S974F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39723967:39723967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913470
CDS Mutation	c.2264T>C
AA Mutation	p.Leu755Ser(p.L755S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39725079:39725079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2524G>A
AA Mutation	p.Val842Ile(p.V842I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39711955:39711955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>A
AA Mutation	p.Ser310Tyr(p.S310Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39723330:39723330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958C>T
AA Mutation	p.Ser653Phe(p.S653F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39717446:39717446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766029214
CDS Mutation	c.1864G>A
AA Mutation	p.Ala622Thr(p.A622T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39724747:39724747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2329G>A
AA Mutation	p.Val777Met(p.V777M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000269571
Start	39724008:39724008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2305G>T
AA Mutation	p.Asp769Tyr(p.D769Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39717417:39717417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1835C>A
AA Mutation	p.Pro612His(p.P612H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39706995:39706995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79A>T
AA Mutation	p.Thr27Ser(p.T27S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39715783:39715783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1357C>A
AA Mutation	p.Leu453Met(p.L453M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39710106:39710106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664G>T
AA Mutation	p.Gly222Cys(p.G222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39708383:39708383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript