Primary Site >> Stomach Cancer

Gene >> RPS6KB2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000312629
Start 67432651:67432651(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780978333
CDS Mutation c.509C>T
AA Mutation p.Thr170Met(p.T170M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000312629
Start 67433392:67433392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.851G>T
AA Mutation p.Gly284Val(p.G284V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000312629
Start 67434420:67434420(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199639577
CDS Mutation c.1091G>A
AA Mutation p.Arg364Gln(p.R364Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000312629
Start 67432983:67432983(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.648C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000312629
Start 67434430:67434430(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202046035
CDS Mutation c.1101G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000312629
Start 67434472:67434472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1143C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000312629
Start 67429225:67429225(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.230delG
AA Mutation p.Gly77AlafsTer22(p.G77Afs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript