Primary Site >> Stomach Cancer

Gene >> TM2D3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000333202
Start 101642546:101642546(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754640606
CDS Mutation c.677C>T
AA Mutation p.Thr226Met(p.T226M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000333202
Start 101646895:101646895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.332A>G
AA Mutation p.Gln111Arg(p.Q111R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000333202
Start 101642495:101642495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.728G>T
AA Mutation p.Gly243Val(p.G243V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000333202
Start 101642518:101642518(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.705T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000333202
Start 101652349:101652349(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.13delG
AA Mutation p.Val5CysfsTer4(p.V5Cfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript