Primary Site >> Stomach Cancer

Gene >> ITM2B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000378565
Start 48256184:48256184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.254A>G
AA Mutation p.Asp85Gly(p.D85G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000378565
Start 48258929:48258929(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756025247
CDS Mutation c.697C>T
AA Mutation p.Arg233Cys(p.R233C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000378565
Start 48261170:48261170(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765077508
CDS Mutation c.747C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000378565
Start 48261185:48261185(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.762T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence inframe_insertion
Transcription ID ENST00000378565
Start 48256296:48256297(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.377_379dupAAG
AA Mutation p.Glu126dup(p.E126dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript