Primary Site >> Stomach Cancer

Gene >> SPAG5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321765
Start 28592468:28592468(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781661528
CDS Mutation c.776G>A
AA Mutation p.Arg259His(p.R259H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321765
Start 28584475:28584475(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375118457
CDS Mutation c.2167C>T
AA Mutation p.Arg723Trp(p.R723W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321765
Start 28592742:28592742(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375467524
CDS Mutation c.502G>A
AA Mutation p.Asp168Asn(p.D168N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321765
Start 28579479:28579479(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2891C>A
AA Mutation p.Pro964Gln(p.P964Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000321765
Start 28592720:28592720(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.524C>G
AA Mutation p.Ala175Gly(p.A175G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000321765
Start 28578516:28578516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3211G>A
AA Mutation p.Glu1071Lys(p.E1071K)
Mutation Classification Missense_Mutation
Feature Type Transcript