Primary Site >> Stomach Cancer

Gene >> SDC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302190
Start 96602504:96602504(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.282G>T
AA Mutation p.Gln94His(p.Q94H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302190
Start 96593574:96593574(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.155C>T
AA Mutation p.Ala52Val(p.A52V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302190
Start 96602465:96602465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.243T>G
AA Mutation p.Ser81Arg(p.S81R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000302190
Start 96608400:96608400(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766386558
CDS Mutation c.372C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000302190
Start 96608334:96608334(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.307-1G>A
Mutation Classification Splice_Site
Feature Type Transcript