Primary Site >> Stomach Cancer

Gene >> SFRP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000220772
Start 41308900:41308900(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.260T>C
AA Mutation p.Met87Thr(p.M87T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000220772
Start 41308790:41308790(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs535023429
CDS Mutation c.370C>T
AA Mutation p.Arg124Trp(p.R124W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000220772
Start 41265366:41265366(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.746A>G
AA Mutation p.Tyr249Cys(p.Y249C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000220772
Start 41308898:41308898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.262G>A
AA Mutation p.Ala88Thr(p.A88T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000220772
Start 41265330:41265330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.782T>C
AA Mutation p.Leu261Pro(p.L261P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000220772
Start 41265171:41265171(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.941A>C
AA Mutation p.Lys314Thr(p.K314T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000220772
Start 41308789:41308789(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.371G>A
AA Mutation p.Arg124Gln(p.R124Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000220772
Start 41303531:41303531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.552G>A
Mutation Classification Silent
Feature Type Transcript