Primary Site >> Stomach Cancer

Gene >> STOML3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379631
Start 38966913:38966913(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.788C>T
AA Mutation p.Thr263Met(p.T263M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379631
Start 38966892:38966892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.809T>C
AA Mutation p.Met270Thr(p.M270T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379631
Start 38970370:38970370(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs34402894
CDS Mutation c.331G>A
AA Mutation p.Val111Ile(p.V111I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379631
Start 38972569:38972569(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.255A>G
AA Mutation p.Ile85Met(p.I85M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379631
Start 38968513:38968513(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753468566
CDS Mutation c.538G>A
AA Mutation p.Glu180Lys(p.E180K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000379631
Start 38970296:38970296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.405T>C
Mutation Classification Silent
Feature Type Transcript