Primary Site >> Stomach Cancer

Gene >> CLEC3B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000296130
Start 45035766:45035766(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.451C>T
AA Mutation p.Arg151Cys(p.R151C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000296130
Start 45035772:45035772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.457G>A
AA Mutation p.Ala153Thr(p.A153T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000296130
Start 45035871:45035871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.556G>A
AA Mutation p.Asp186Asn(p.D186N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000296130
Start 45035558:45035558(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.243C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000296130
Start 45035762:45035762(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.447C>T
Mutation Classification Silent
Feature Type Transcript