Primary Site >> Stomach Cancer

Gene >> AGO4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000373210
Start 35822884:35822884(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773809553
CDS Mutation c.208C>T
AA Mutation p.Arg70Trp(p.R70W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000373210
Start 35831572:35831572(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.994G>A
AA Mutation p.Glu332Lys(p.E332K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000373210
Start 35825425:35825425(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.419A>G
AA Mutation p.His140Arg(p.H140R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000373210
Start 35822879:35822879(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.203T>C
AA Mutation p.Met68Thr(p.M68T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000373210
Start 35835954:35835954(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1685A>G
AA Mutation p.Lys562Arg(p.K562R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000373210
Start 35853541:35853541(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2522C>T
AA Mutation p.Pro841Leu(p.P841L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000373210
Start 35841679:35841679(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2104C>T
AA Mutation p.Pro702Ser(p.P702S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000373210
Start 35825715:35825715(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs535953094
CDS Mutation c.525G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000373210
Start 35841216:35841216(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1781delC
AA Mutation p.Pro594GlnfsTer51(p.P594Qfs*51)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000373210
Start 35841199:35841199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1759G>T
AA Mutation p.Gly587Ter(p.G587*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000373210
Start 35841352:35841352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1912C>T
AA Mutation p.Gln638Ter(p.Q638*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000373210
Start 35831426:35831427(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.852dupT
AA Mutation p.Pro285SerfsTer19(p.P285Sfs*19)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000373210
Start 35817043:35817059(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.185+1_185+17delGTAAGGATTAGAAACAG
Mutation Classification Splice_Site
Feature Type Transcript