Primary Site >> Stomach Cancer

Gene >> KMO

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000366559
Start 241586680:241586680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.959G>T
AA Mutation p.Gly320Val(p.G320V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366559
Start 241562247:241562247(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.530T>A
AA Mutation p.Leu177Gln(p.L177Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366559
Start 241562214:241562214(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.497G>A
AA Mutation p.Cys166Tyr(p.C166Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000366559
Start 241592115:241592115(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1423G>T
AA Mutation p.Asp475Tyr(p.D475Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000366559
Start 241565042:241565042(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.671T>A
AA Mutation p.Ile224Asn(p.I224N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000366559
Start 241566593:241566593(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.790G>A
AA Mutation p.Ala264Thr(p.A264T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000366559
Start 241568635:241568635(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.945A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000366559
Start 241549684:241549684(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.132A>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000366559
Start 241590256:241590256(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1259delA
AA Mutation p.Lys420ArgfsTer2(p.K420Rfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000366559
Start 241590043:241590043(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1134delT
AA Mutation p.Gln379ArgfsTer28(p.Q379Rfs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000366559
Start 241590255:241590256(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1259dupA
AA Mutation p.Val421GlyfsTer65(p.V421Gfs*65)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript