Primary Site >> Stomach Cancer

Gene >> G3BP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359707
Start 75645593:75645593(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1286G>A
AA Mutation p.Arg429His(p.R429H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359707
Start 75657729:75657729(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.179A>T
AA Mutation p.Asp60Val(p.D60V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359707
Start 75645608:75645608(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1271G>T
AA Mutation p.Arg424Leu(p.R424L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359707
Start 75646391:75646391(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1123G>C
AA Mutation p.Gly375Arg(p.G375R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359707
Start 75661989:75661989(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.37C>T
AA Mutation p.Arg13Trp(p.R13W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000359707
Start 75645583:75645583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1296A>G
Mutation Classification Silent
Feature Type Transcript