Primary Site >> Stomach Cancer

Gene >> CCDC116

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000292779
Start 21634368:21634368(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764612340
CDS Mutation c.419C>T
AA Mutation p.Pro140Leu(p.P140L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000292779
Start 21634908:21634908(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.845A>C
AA Mutation p.Gln282Pro(p.Q282P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000292779
Start 21636922:21636922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1694T>C
AA Mutation p.Met565Thr(p.M565T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000292779
Start 21635087:21635087(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1024C>A
AA Mutation p.Pro342Thr(p.P342T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000292779
Start 21635097:21635097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1034A>G
AA Mutation p.Asp345Gly(p.D345G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000292779
Start 21634201:21634201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.252C>A
AA Mutation p.Asp84Glu(p.D84E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000292779
Start 21634692:21634692(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.629T>C
AA Mutation p.Leu210Pro(p.L210P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000292779
Start 21635002:21635002(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.939G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000292779
Start 21634042:21634042(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.93A>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000292779
Start 21634228:21634228(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778183454
CDS Mutation c.279G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000292779
Start 21634816:21634816(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370484007
CDS Mutation c.753C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000292779
Start 21635059:21635059(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.996C>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000292779
Start 21634960:21634960(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.897C>G
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000292779
Start 21636737:21636737(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1509G>A
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000292779
Start 21637007:21637007(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1779T>C
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000292779
Start 21636762:21636763(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1537dupC
AA Mutation p.Arg513ProfsTer72(p.R513Pfs*72)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript