Primary Site >> Stomach Cancer

Gene >> NTN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9023038:9023038(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.665C>T
AA Mutation p.Thr222Met(p.T222M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9022879:9022879(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.506G>A
AA Mutation p.Arg169His(p.R169H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9162846:9162846(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs531668666
CDS Mutation c.1052G>A
AA Mutation p.Arg351His(p.R351H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9162909:9162909(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1115G>A
AA Mutation p.Arg372His(p.R372H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9182933:9182933(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376278603
CDS Mutation c.1375C>A
AA Mutation p.Pro459Thr(p.P459T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9022795:9022795(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.422A>C
AA Mutation p.Lys141Thr(p.K141T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9022899:9022899(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.526T>C
AA Mutation p.Phe176Leu(p.F176L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9023302:9023302(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.929C>T
AA Mutation p.Thr310Met(p.T310M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000173229
Start 9022701:9022701(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.328G>A
AA Mutation p.Asp110Asn(p.D110N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000173229
Start 9023195:9023195(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.822C>T
Mutation Classification Silent
Feature Type Transcript