Primary Site >> Stomach Cancer

Gene >> SLCO2B1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000289575
Start 75203421:75203421(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs547836651
CDS Mutation c.1943G>A
AA Mutation p.Arg648Gln(p.R648Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000289575
Start 75165866:75165866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.365C>A
AA Mutation p.Ala122Asp(p.A122D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000289575
Start 75165863:75165863(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.362G>T
AA Mutation p.Gly121Val(p.G121V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000289575
Start 75165935:75165935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.434A>G
AA Mutation p.Asp145Gly(p.D145G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000289575
Start 75200309:75200309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1685T>C
AA Mutation p.Val562Ala(p.V562A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000289575
Start 75202928:75202928(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1791G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000289575
Start 75169688:75169703(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.706_721delATGGGGCCAGGCCTGG
AA Mutation p.Met236ProfsTer25(p.M236Pfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript