Primary Site >> Stomach Cancer

Gene >> TTC12

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000529221
Start 113325583:113325583(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372770355
CDS Mutation c.382C>T
AA Mutation p.Arg128Cys(p.R128C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000529221
Start 113339375:113339375(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs532510819
CDS Mutation c.727G>A
AA Mutation p.Val243Met(p.V243M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000529221
Start 113362425:113362425(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1639A>G
AA Mutation p.Thr547Ala(p.T547A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000529221
Start 113324677:113324677(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145843861
CDS Mutation c.317C>T
AA Mutation p.Ala106Val(p.A106V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000529221
Start 113352098:113352098(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147647661
CDS Mutation c.1337C>T
AA Mutation p.Ser446Leu(p.S446L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000529221
Start 113344406:113344406(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370336232
CDS Mutation c.1120C>T
AA Mutation p.Arg374Trp(p.R374W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000529221
Start 113344355:113344355(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs555704558
CDS Mutation c.1069C>T
AA Mutation p.Arg357Trp(p.R357W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000529221
Start 113339323:113339323(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.675C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000529221
Start 113364908:113364908(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1890T>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000529221
Start 113350085:113350085(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1167G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000529221
Start 113339438:113339438(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.795delG
AA Mutation p.Ile266LeufsTer4(p.I266Lfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000529221
Start 113324662:113324662(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.305delA
AA Mutation p.Asn102ThrfsTer8(p.N102Tfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000529221
Start 113359450:113359450(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1536delT
AA Mutation p.Phe512LeufsTer10(p.F512Lfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000529221
Start 113316297:113316297(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.40A>T
AA Mutation p.Lys14Ter(p.K14*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000529221
Start 113329919:113329919(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.445-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 16
Mutation Consequence splice_donor_variant
Transcription ID ENST00000529221
Start 113352208:113352208(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1446+1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 17
Mutation Consequence splice_acceptor_variant;coding_sequence_variant
Transcription ID ENST00000529221
Start 113324603:113324611(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.245-2_251delAGAGGCCTT
Mutation Classification Splice_Site
Feature Type Transcript