Primary Site >> Stomach Cancer

Gene >> REN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000272190
Start 204155864:204155864(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1015G>A
AA Mutation p.Gly339Arg(p.G339R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000272190
Start 204156713:204156713(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.782T>C
AA Mutation p.Leu261Pro(p.L261P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000272190
Start 204156720:204156720(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.775A>G
AA Mutation p.Ile259Val(p.I259V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000272190
Start 204155084:204155084(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1153T>A
AA Mutation p.Phe385Ile(p.F385I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000272190
Start 204161309:204161309(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376156157
CDS Mutation c.356G>A
AA Mutation p.Arg119His(p.R119H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000272190
Start 204156258:204156258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.880G>A
AA Mutation p.Gly294Ser(p.G294S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000272190
Start 204155067:204155067(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1170C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000272190
Start 204162061:204162061(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.201G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000272190
Start 204155829:204155830(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1049_1050delAT
AA Mutation p.Tyr350CysfsTer8(p.Y350Cfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript