Primary Site >> Stomach Cancer

Gene >> ALOX15

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000293761
Start 4637124:4637124(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.942G>A
AA Mutation p.Met314Ile(p.M314I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000293761
Start 4633215:4633215(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776154712
CDS Mutation c.1349G>A
AA Mutation p.Arg450Gln(p.R450Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000293761
Start 4631983:4631983(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761098208
CDS Mutation c.1715C>T
AA Mutation p.Thr572Met(p.T572M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000293761
Start 4631640:4631640(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1949A>G
AA Mutation p.Tyr650Cys(p.Y650C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000293761
Start 4633415:4633415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1247A>G
AA Mutation p.Gln416Arg(p.Q416R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000293761
Start 4632014:4632014(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770448397
CDS Mutation c.1684C>T
AA Mutation p.Arg562Trp(p.R562W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000293761
Start 4633254:4633254(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1310C>A
AA Mutation p.Thr437Asn(p.T437N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000293761
Start 4635952:4635952(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.968delC
AA Mutation p.Thr323LysfsTer40(p.T323Kfs*40)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000293761
Start 4641543:4641544(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.108dupG
AA Mutation p.Lys37GlufsTer36(p.K37Efs*36)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 10
Mutation Consequence splice_donor_variant
Transcription ID ENST00000293761
Start 4635757:4635757(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1161+2T>C
Mutation Classification Splice_Site
Feature Type Transcript