Primary Site >> Stomach Cancer

Gene >> TRAK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201387874:201387874(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151088733
CDS Mutation c.1525C>T
AA Mutation p.Arg509Trp(p.R509W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201387925:201387925(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758212070
CDS Mutation c.1474C>T
AA Mutation p.Arg492Cys(p.R492C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201407481:201407481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.208A>G
AA Mutation p.Thr70Ala(p.T70A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201389403:201389403(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1294C>T
AA Mutation p.Arg432Cys(p.R432C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201381070:201381070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2218A>T
AA Mutation p.Ser740Cys(p.S740C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201399400:201399400(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.457C>G
AA Mutation p.Gln153Glu(p.Q153E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201387778:201387778(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1621A>T
AA Mutation p.Ile541Phe(p.I541F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201401086:201401086(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.295A>G
AA Mutation p.Thr99Ala(p.T99A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201394854:201394854(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.919G>A
AA Mutation p.Glu307Lys(p.E307K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000332624
Start 201395420:201395420(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.794G>C
AA Mutation p.Arg265Thr(p.R265T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000332624
Start 201393010:201393010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1012G>T
AA Mutation p.Gly338Ter(p.G338*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript