Primary Site >> Stomach Cancer

Gene >> ANXA11

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372231
Start 80166103:80166103(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.839A>C
AA Mutation p.Glu280Ala(p.E280A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372231
Start 80167247:80167247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768664021
CDS Mutation c.628C>T
AA Mutation p.Arg210Trp(p.R210W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372231
Start 80164101:80164101(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.901T>A
AA Mutation p.Ser301Thr(p.S301T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000372231
Start 80155866:80155866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1505G>A
AA Mutation p.Gly502Asp(p.G502D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000372231
Start 80157707:80157707(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374382845
CDS Mutation c.1392C>T
Mutation Classification Silent
Feature Type Transcript