Primary Site >> Stomach Cancer

Gene >> SFRP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000274063
Start 153788511:153788511(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533800119
CDS Mutation c.325G>A
AA Mutation p.Glu109Lys(p.E109K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000274063
Start 153781749:153781749(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.590A>C
AA Mutation p.Lys197Thr(p.K197T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000274063
Start 153781516:153781516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.823C>T
AA Mutation p.Arg275Trp(p.R275W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000274063
Start 153788661:153788661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.175C>T
AA Mutation p.Arg59Trp(p.R59W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000274063
Start 153788440:153788440(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.396C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000274063
Start 153788686:153788686(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.150C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000274063
Start 153788362:153788362(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.474C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000274063
Start 153788373:153788373(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.463delC
AA Mutation p.Leu155SerfsTer31(p.L155Sfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000274063
Start 153781594:153781594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.745G>T
AA Mutation p.Glu249Ter(p.E249*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript