Primary Site >> Stomach Cancer

Gene >> XRCC5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000392132
Start 216127625:216127625(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.888C>G
AA Mutation p.Cys296Trp(p.C296W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000392132
Start 216148164:216148164(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761811665
CDS Mutation c.1558G>A
AA Mutation p.Ala520Thr(p.A520T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000392132
Start 216137161:216137161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1187C>T
AA Mutation p.Ala396Val(p.A396V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000392132
Start 216204352:216204352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2140G>A
AA Mutation p.Asp714Asn(p.D714N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000392132
Start 216122165:216122165(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.595G>A
AA Mutation p.Glu199Lys(p.E199K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000392132
Start 216127588:216127588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.851T>A
AA Mutation p.Leu284Gln(p.L284Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000392132
Start 216116832:216116832(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768296550
CDS Mutation c.309A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000392132
Start 216127589:216127589(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.858delA
AA Mutation p.Glu287LysfsTer11(p.E287Kfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000392132
Start 216127628:216127628(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.893delA
AA Mutation p.Asn298MetfsTer9(p.N298Mfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000392132
Start 216160090:216160090(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1698delA
AA Mutation p.Lys566AsnfsTer2(p.K566Nfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000392132
Start 216132352:216132352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1078C>T
AA Mutation p.Gln360Ter(p.Q360*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript