Primary Site >> Stomach Cancer

Gene >> TRIM28

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000253024
Start 58549554:58549554(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1886G>A
AA Mutation p.Arg629His(p.R629H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000253024
Start 58549839:58549839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2085G>T
AA Mutation p.Lys695Asn(p.K695N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000253024
Start 58550181:58550181(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2228T>C
AA Mutation p.Ile743Thr(p.I743T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000253024
Start 58547815:58547815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.863A>G
AA Mutation p.Gln288Arg(p.Q288R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000253024
Start 58550217:58550217(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2264A>G
AA Mutation p.Tyr755Cys(p.Y755C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000253024
Start 58547459:58547459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.670T>C
AA Mutation p.Cys224Arg(p.C224R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000253024
Start 58549161:58549161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1583C>A
AA Mutation p.Ala528Asp(p.A528D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000253024
Start 58549331:58549331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1663G>C
AA Mutation p.Glu555Gln(p.E555Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000253024
Start 58548109:58548109(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1030C>T
AA Mutation p.His344Tyr(p.H344Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000253024
Start 58549117:58549117(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1539C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000253024
Start 58545835:58545835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.525G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000253024
Start 58549052:58549053(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1474_1475insA
AA Mutation p.Arg492GlnfsTer9(p.R492Qfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript