Primary Site >> Stomach Cancer

Gene >> ZNF382

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36627279:36627279(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1382A>G
AA Mutation p.Glu461Gly(p.E461G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36626223:36626223(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.326T>G
AA Mutation p.Leu109Arg(p.L109R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36627294:36627294(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1397G>T
AA Mutation p.Cys466Phe(p.C466F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36626773:36626773(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.876A>C
AA Mutation p.Glu292Asp(p.E292D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36627143:36627143(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1246G>A
AA Mutation p.Ala416Thr(p.A416T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36626264:36626264(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.367C>A
AA Mutation p.Leu123Ile(p.L123I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36627072:36627072(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1175A>C
AA Mutation p.Lys392Thr(p.K392T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36627402:36627402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1505G>C
AA Mutation p.Ser502Thr(p.S502T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36626221:36626221(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.324A>C
AA Mutation p.Lys108Asn(p.K108N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000292928
Start 36627375:36627375(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1478G>A
AA Mutation p.Gly493Glu(p.G493E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000292928
Start 36609992:36609992(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.78T>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000292928
Start 36626755:36626755(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.858T>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000292928
Start 36627274:36627274(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1381delG
AA Mutation p.Glu461LysfsTer84(p.E461Kfs*84)
Mutation Classification Frame_Shift_Del
Feature Type Transcript