Primary Site >> Stomach Cancer

Gene >> LARP7

ID 1
Mutation Consequence coding_sequence_variant;3_prime_UTR_variant
Transcription ID ENST00000324052
Start 112657327:112657328(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.*8_*9delAA
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324052
Start 112646903:112646903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.500G>A
AA Mutation p.Gly167Glu(p.G167E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000324052
Start 112653236:112653236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1576G>A
AA Mutation p.Gly526Ser(p.G526S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000324052
Start 112646658:112646658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.374G>A
AA Mutation p.Arg125His(p.R125H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000324052
Start 112649598:112649598(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs763740398
CDS Mutation c.1213delA
AA Mutation p.Thr405GlnfsTer5(p.T405Qfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000324052
Start 112644740:112644740(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs781724052
CDS Mutation c.77delA
AA Mutation p.Lys26ArgfsTer36(p.K26Rfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000324052
Start 112646388:112646389(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.246dupA
AA Mutation p.Leu83IlefsTer4(p.L83Ifs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript