Primary Site >> Stomach Cancer

Gene >> SPP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395080
Start 87981488:87981488(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.230A>C
AA Mutation p.Lys77Thr(p.K77T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395080
Start 87981499:87981499(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.241A>C
AA Mutation p.Ser81Arg(p.S81R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395080
Start 87977088:87977088(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.84G>T
AA Mutation p.Glu28Asp(p.E28D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395080
Start 87982782:87982782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.831A>T
AA Mutation p.Glu277Asp(p.E277D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395080
Start 87982504:87982504(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.553A>G
AA Mutation p.Thr185Ala(p.T185A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000395080
Start 87982608:87982608(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.657C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000395080
Start 87981687:87981687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.429C>T
Mutation Classification Silent
Feature Type Transcript