Primary Site >> Stomach Cancer

Gene >> ITM2C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000326427
Start 230877545:230877545(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150758684
CDS Mutation c.707G>A
AA Mutation p.Arg236Gln(p.R236Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000326427
Start 230877543:230877543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376535631
CDS Mutation c.705G>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000326427
Start 230876961:230876961(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761621617
CDS Mutation c.555C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000326427
Start 230875769:230875769(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs544434687
CDS Mutation c.411C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000326427
Start 230877453:230877453(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780377757
CDS Mutation c.615G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000326427
Start 230875664:230875664(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.306C>T
Mutation Classification Silent
Feature Type Transcript