Primary Site >> Stomach Cancer

Gene >> SC5D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264027
Start 121303382:121303382(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7C>T
AA Mutation p.Leu3Phe(p.L3F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264027
Start 121303411:121303411(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.36T>G
AA Mutation p.Phe12Leu(p.F12L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264027
Start 121307498:121307498(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.886A>G
AA Mutation p.Thr296Ala(p.T296A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264027
Start 121307253:121307253(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148689830
CDS Mutation c.641G>A
AA Mutation p.Arg214His(p.R214H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264027
Start 121307157:121307157(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.545T>C
AA Mutation p.Ile182Thr(p.I182T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000264027
Start 121307407:121307407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.795G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000264027
Start 121303408:121303408(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.39delT
AA Mutation p.Phe13LeufsTer23(p.F13Lfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000264027
Start 121307056:121307056(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.445-1G>A
Mutation Classification Splice_Site
Feature Type Transcript