Primary Site >> Stomach Cancer

Gene >> CACNB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394303
Start 39187577:39187577(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141548672
CDS Mutation c.316C>T
AA Mutation p.Arg106Trp(p.R106W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394303
Start 39184842:39184842(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.671A>G
AA Mutation p.Asp224Gly(p.D224G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394303
Start 39194889:39194889(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.166C>T
AA Mutation p.Arg56Cys(p.R56C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000394303
Start 39175296:39175296(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779856110
CDS Mutation c.1694G>A
AA Mutation p.Arg565Gln(p.R565Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000394303
Start 39187530:39187530(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.363G>A
Mutation Classification Silent
Feature Type Transcript