Primary Site >> Stomach Cancer

Gene >> ZNF79

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127435163:127435163(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs192043906
CDS Mutation c.179G>A
AA Mutation p.Arg60Gln(p.R60Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127444695:127444695(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.995C>A
AA Mutation p.Pro332His(p.P332H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127444322:127444322(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.622C>G
AA Mutation p.Leu208Val(p.L208V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000342483
Start 127444031:127444031(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs182450731
CDS Mutation c.331T>C
AA Mutation p.Trp111Arg(p.W111R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127444937:127444937(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148709335
CDS Mutation c.1237G>A
AA Mutation p.Gly413Arg(p.G413R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127428906:127428906(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.91A>G
AA Mutation p.Thr31Ala(p.T31A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127445148:127445148(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370158712
CDS Mutation c.1448G>A
AA Mutation p.Arg483Gln(p.R483Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127444508:127444508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.808A>G
AA Mutation p.Thr270Ala(p.T270A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127444183:127444183(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.483G>T
AA Mutation p.Gln161His(p.Q161H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000342483
Start 127444824:127444824(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1124A>G
AA Mutation p.Asn375Ser(p.N375S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000342483
Start 127444381:127444381(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.681G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000342483
Start 127445033:127445034(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1334_1335delAT
AA Mutation p.Tyr445Ter(p.Y445*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000342483
Start 127435088:127435088(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.106-2A>G
Mutation Classification Splice_Site
Feature Type Transcript