Primary Site >> Stomach Cancer

Gene >> DYRK3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367109
Start 206648648:206648648(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1450G>A
AA Mutation p.Gly484Arg(p.G484R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367109
Start 206648081:206648081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.883C>A
AA Mutation p.Leu295Ile(p.L295I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367109
Start 206647731:206647731(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.533G>T
AA Mutation p.Arg178Ile(p.R178I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000367109
Start 206647785:206647785(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.587C>T
AA Mutation p.Ala196Val(p.A196V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000367109
Start 206647803:206647803(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.605G>A
AA Mutation p.Arg202Gln(p.R202Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000367109
Start 206648929:206648929(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1731A>G
AA Mutation p.Ile577Met(p.I577M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000367109
Start 206648600:206648600(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782350176
CDS Mutation c.1402C>T
AA Mutation p.Arg468Cys(p.R468C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000367109
Start 206647780:206647780(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.582T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000367109
Start 206648096:206648096(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.905delA
AA Mutation p.Asn302IlefsTer35(p.N302Ifs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000367109
Start 206647427:206647427(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.233delT
AA Mutation p.Leu78TrpfsTer6(p.L78Wfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000367109
Start 206647697:206647697(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.499G>T
AA Mutation p.Glu167Ter(p.E167*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000367109
Start 206647892:206647892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.694C>T
AA Mutation p.Arg232Ter(p.R232*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000367109
Start 206648962:206648963(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1765dupT
AA Mutation p.Ter589Leu(p.*589L)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript