Primary Site >> Stomach Cancer

Gene >> C4B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000435363
Start 32029761:32029761(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776621861
CDS Mutation c.3872G>A
AA Mutation p.Arg1291His(p.R1291H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000435363
Start 32029623:32029623(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746665484
CDS Mutation c.3734C>T
AA Mutation p.Pro1245Leu(p.P1245L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000435363
Start 32028717:32028717(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3255C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000435363
Start 32027105:32027105(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2575C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000435363
Start 32028804:32028804(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377359889
CDS Mutation c.3342C>T
Mutation Classification Silent
Feature Type Transcript