Primary Site >> Stomach Cancer

Gene >> ZNF699

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000308650
Start 9296271:9296271(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1133T>C
AA Mutation p.Leu378Pro(p.L378P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000308650
Start 9295901:9295901(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1503G>T
AA Mutation p.Lys501Asn(p.K501N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000308650
Start 9297951:9297951(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.215A>T
AA Mutation p.Glu72Val(p.E72V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000308650
Start 9295930:9295930(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757840909
CDS Mutation c.1474G>A
AA Mutation p.Glu492Lys(p.E492K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000308650
Start 9296718:9296718(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.686G>T
AA Mutation p.Gly229Val(p.G229V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000308650
Start 9295998:9295998(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1406A>C
AA Mutation p.His469Pro(p.H469P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000308650
Start 9296293:9296293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1111G>A
AA Mutation p.Ala371Thr(p.A371T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000308650
Start 9296823:9296823(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.581C>T
AA Mutation p.Ser194Phe(p.S194F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000308650
Start 9296425:9296425(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.979A>C
Mutation Classification Silent
Feature Type Transcript