Primary Site >> Stomach Cancer

Gene >> SPOP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000347630
Start 49607301:49607301(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.786G>T
AA Mutation p.Lys262Asn(p.K262N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000347630
Start 49622008:49622008(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.138G>T
AA Mutation p.Glu46Asp(p.E46D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000347630
Start 49601941:49601941(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.904G>A
AA Mutation p.Ala302Thr(p.A302T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000347630
Start 49619291:49619291(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.295C>T
AA Mutation p.Arg99Trp(p.R99W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000347630
Start 49622787:49622787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.24A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000347630
Start 49601984:49601984(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.861C>T
Mutation Classification Silent
Feature Type Transcript