Primary Site >> Stomach Cancer

Gene >> CA9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000378357
Start 35680813:35680813(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151268469
CDS Mutation c.1298T>C
AA Mutation p.Val433Ala(p.V433A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000378357
Start 35674220:35674220(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.261G>T
AA Mutation p.Glu87Asp(p.E87D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000378357
Start 35675764:35675764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.437A>T
AA Mutation p.Asp146Val(p.D146V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000378357
Start 35676369:35676369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.820G>A
AA Mutation p.Val274Met(p.V274M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000378357
Start 35676316:35676316(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.767G>A
AA Mutation p.Ser256Asn(p.S256N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000378357
Start 35676074:35676074(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.615C>A
Mutation Classification Silent
Feature Type Transcript