Primary Site >> Stomach Cancer

Gene >> NEIL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355059
Start 75354268:75354268(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751648947
CDS Mutation c.865G>A
AA Mutation p.Ala289Thr(p.A289T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355059
Start 75348934:75348934(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.29C>T
AA Mutation p.Ala10Val(p.A10V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000355059
Start 75353764:75353764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.744C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000355059
Start 75352333:75352333(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.570delC
AA Mutation p.Phe191LeufsTer20(p.F191Lfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000355059
Start 75349240:75349241(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.336_337delAT
AA Mutation p.Cys113PhefsTer42(p.C113Ffs*42)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000355059
Start 75349226:75349226(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.325delC
AA Mutation p.Arg109GlyfsTer44(p.R109Gfs*44)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000355059
Start 75349206:75349206(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.304delT
AA Mutation p.Tyr102ThrfsTer51(p.Y102Tfs*51)
Mutation Classification Frame_Shift_Del
Feature Type Transcript