Primary Site >> Stomach Cancer

Gene >> FOXL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000320241
Start 86578916:86578916(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.193G>A
AA Mutation p.Ala65Thr(p.A65T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000320241
Start 86578941:86578941(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.218A>G
AA Mutation p.Asn73Ser(p.N73S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000320241
Start 86578904:86578904(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.181G>T
AA Mutation p.Ala61Ser(p.A61S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000320241
Start 86579073:86579073(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.350C>T
AA Mutation p.Pro117Leu(p.P117L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000320241
Start 86579617:86579617(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.894G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000320241
Start 86578864:86578864(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.141G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000320241
Start 86578783:86578783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.60G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000320241
Start 86578768:86578768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.45G>A
Mutation Classification Silent
Feature Type Transcript