Primary Site >> Stomach Cancer

Gene >> MYB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367814
Start 135193881:135193881(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778761961
CDS Mutation c.806T>C
AA Mutation p.Ile269Thr(p.I269T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367814
Start 135185985:135185985(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776200677
CDS Mutation c.106C>T
AA Mutation p.Arg36Cys(p.R36C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367814
Start 135195808:135195808(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772410551
CDS Mutation c.1009A>G
AA Mutation p.Arg337Gly(p.R337G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000367814
Start 135195870:135195870(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1071G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000367814
Start 135217974:135217974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1917C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000367814
Start 135200115:135200115(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1377C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000367814
Start 135198969:135198969(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1270delC
AA Mutation p.Leu424SerfsTer6(p.L424Sfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript