Primary Site >> Stomach Cancer

Gene >> RAPGEF3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000389212
Start 47740172:47740172(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767312809
CDS Mutation c.2342G>A
AA Mutation p.Arg781Gln(p.R781Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000389212
Start 47749515:47749515(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.916G>A
AA Mutation p.Glu306Lys(p.E306K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000389212
Start 47739158:47739158(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763136670
CDS Mutation c.2446C>T
AA Mutation p.Pro816Ser(p.P816S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000389212
Start 47739212:47739212(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753781665
CDS Mutation c.2392C>T
AA Mutation p.Arg798Trp(p.R798W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000389212
Start 47747734:47747734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1451C>A
AA Mutation p.Pro484His(p.P484H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000389212
Start 47740359:47740359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2268C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000389212
Start 47738720:47738720(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2496A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000389212
Start 47740951:47740951(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2013G>A
Mutation Classification Silent
Feature Type Transcript