Primary Site >> Stomach Cancer

Gene >> LARP4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000398473
Start 50467083:50467083(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1508G>T
AA Mutation p.Arg503Met(p.R503M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000398473
Start 50453514:50453514(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.859G>A
AA Mutation p.Asp287Asn(p.D287N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000398473
Start 50453617:50453617(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.962G>T
AA Mutation p.Ser321Ile(p.S321I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000398473
Start 50441630:50441630(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.791G>A
AA Mutation p.Gly264Asp(p.G264D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000398473
Start 50427774:50427774(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.31A>G
AA Mutation p.Lys11Glu(p.K11E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000398473
Start 50462602:50462602(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748279624
CDS Mutation c.1355G>A
AA Mutation p.Arg452Gln(p.R452Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000398473
Start 50473459:50473459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1590G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000398473
Start 50453486:50453486(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.831T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000398473
Start 50454408:50454408(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1118delA
AA Mutation p.Asn373IlefsTer3(p.N373Ifs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000398473
Start 50454407:50454408(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1118dupA
AA Mutation p.Asn373LysfsTer8(p.N373Kfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000398473
Start 50453483:50453484(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.834dupT
AA Mutation p.Ala279CysfsTer2(p.A279Cfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript