Primary Site >> Stomach Cancer

Gene >> RAD18

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264926
Start 8958946:8958946(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.107T>C
AA Mutation p.Met36Thr(p.M36T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264926
Start 8902445:8902445(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1103C>T
AA Mutation p.Ser368Leu(p.S368L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264926
Start 8948549:8948549(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.155A>C
AA Mutation p.Lys52Thr(p.K52T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264926
Start 8890443:8890443(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1331C>T
AA Mutation p.Ser444Leu(p.S444L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264926
Start 8935907:8935907(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.853T>C
AA Mutation p.Tyr285His(p.Y285H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000264926
Start 8941723:8941723(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.348A>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264926
Start 8958981:8958981(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.72G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000264926
Start 8902437:8902437(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1111delA
AA Mutation p.Thr371GlnfsTer2(p.T371Qfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000264926
Start 8941617:8941617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.454G>T
AA Mutation p.Glu152Ter(p.E152*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript