Primary Site >> Stomach Cancer

Gene >> DMTF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000331242
Start 87194726:87194726(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2071A>G
AA Mutation p.Ile691Val(p.I691V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000331242
Start 87194778:87194778(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2123C>T
AA Mutation p.Ala708Val(p.A708V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000331242
Start 87182265:87182265(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.748G>T
AA Mutation p.Gly250Trp(p.G250W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000331242
Start 87195032:87195032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2175T>A
AA Mutation p.Asp725Glu(p.D725E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000331242
Start 87184453:87184453(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.877A>G
AA Mutation p.Ser293Gly(p.S293G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000331242
Start 87194694:87194694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2039C>A
AA Mutation p.Ser680Tyr(p.S680Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000331242
Start 87184540:87184540(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.964C>T
AA Mutation p.Arg322Cys(p.R322C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000331242
Start 87184522:87184522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.946C>T
AA Mutation p.Arg316Cys(p.R316C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000331242
Start 87188109:87188109(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1219A>G
AA Mutation p.Lys407Glu(p.K407E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000331242
Start 87182309:87182309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.792C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000331242
Start 87188128:87188128(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1244delA
AA Mutation p.Asn415ThrfsTer28(p.N415Tfs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000331242
Start 87184418:87184419(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.844_845delAA
AA Mutation p.Lys282GlufsTer8(p.K282Efs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript