Mutation

Primary Site >> Stomach Cancer

Gene >> NEU2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233032783:233032783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753794682
CDS Mutation	c.112G>A
AA Mutation	p.Ala38Thr(p.A38T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034906:233034906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992G>A
AA Mutation	p.Ser331Asn(p.S331N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034446:233034446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532G>A
AA Mutation	p.Ala178Thr(p.A178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034544:233034544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630C>A
AA Mutation	p.His210Gln(p.H210Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233032705:233032705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778630184
CDS Mutation	c.34G>A
AA Mutation	p.Val12Met(p.V12M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034126:233034126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212A>C
AA Mutation	p.Gln71Pro(p.Q71P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233840
Start	233034853:233034853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748592888
CDS Mutation	c.939G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233840
Start	233034280:233034280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762359314
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233840
Start	233034202:233034202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763884669
CDS Mutation	c.288G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233840
Start	233032785:233032785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747879605
CDS Mutation	c.114G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233840
Start	233034775:233034775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233840
Start	233034954:233034954(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1044delC
AA Mutation	p.Leu349CysfsTer21(p.L349Cfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233840
Start	233034757:233034757(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.847delC
AA Mutation	p.Arg283AlafsTer87(p.R283Afs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript