Primary Site >> Stomach Cancer

Gene >> CCDC136

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297788
Start 128812206:128812206(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2435T>G
AA Mutation p.Ile812Ser(p.I812S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297788
Start 128812047:128812047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2276G>A
AA Mutation p.Arg759His(p.R759H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297788
Start 128807394:128807394(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1454A>T
AA Mutation p.Lys485Met(p.K485M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000297788
Start 128805831:128805831(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756674345
CDS Mutation c.1019G>A
AA Mutation p.Arg340Gln(p.R340Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000297788
Start 128814740:128814740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2866C>G
AA Mutation p.Gln956Glu(p.Q956E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000297788
Start 128814717:128814717(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2843T>C
AA Mutation p.Val948Ala(p.V948A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000297788
Start 128801299:128801299(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773067584
CDS Mutation c.460C>T
AA Mutation p.Arg154Trp(p.R154W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000297788
Start 128801319:128801319(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776548870
CDS Mutation c.480C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000297788
Start 128811991:128811991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2220C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000297788
Start 128807515:128807515(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1575T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000297788
Start 128814670:128814670(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2796G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000297788
Start 128811890:128811890(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2121delG
AA Mutation p.Arg708GlyfsTer3(p.R708Gfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence inframe_insertion
Transcription ID ENST00000297788
Start 128812207:128812208(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2437_2438insAATGCA
AA Mutation p.Ile812_Thr813insLysCys(p.I812_T813insKC)
Mutation Classification In_Frame_Ins
Feature Type Transcript