Primary Site >> Stomach Cancer

Gene >> XRCC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359321
Start 152648938:152648938(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.547C>T
AA Mutation p.Leu183Phe(p.L183F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359321
Start 152649285:152649285(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.200T>C
AA Mutation p.Leu67Pro(p.L67P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000359321
Start 152648804:152648804(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.681C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000359321
Start 152648861:152648861(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.624A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000359321
Start 152648675:152648675(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.810delT
AA Mutation p.Phe270LeufsTer27(p.F270Lfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000359321
Start 152648684:152648684(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.801delA
AA Mutation p.Lys267AsnfsTer30(p.K267Nfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000359321
Start 152649135:152649135(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.350delT
AA Mutation p.Leu117TrpfsTer17(p.L117Wfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000359321
Start 152648674:152648675(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.810dupT
AA Mutation p.Ile271TyrfsTer8(p.I271Yfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript