Primary Site >> Esophagus Cancer

Gene >> ZNF208

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21972753:21972753(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2281T>C
AA Mutation p.Ser761Pro(p.S761P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21973871:21973871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1163A>G
AA Mutation p.Lys388Arg(p.K388R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21972371:21972371(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2663C>A
AA Mutation p.Pro888His(p.P888H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21974010:21974010(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1024A>C
AA Mutation p.Lys342Gln(p.K342Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21972392:21972392(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs572727442
CDS Mutation c.2642A>T
AA Mutation p.Lys881Ile(p.K881I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21974663:21974663(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.371A>C
AA Mutation p.Lys124Thr(p.K124T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21973198:21973198(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs553606877
CDS Mutation c.1836A>C
AA Mutation p.Glu612Asp(p.E612D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21974024:21974024(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1010G>T
AA Mutation p.Gly337Val(p.G337V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21972227:21972227(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2807A>T
AA Mutation p.Lys936Met(p.K936M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21973319:21973319(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1715A>C
AA Mutation p.Lys572Thr(p.K572T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21974353:21974353(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.681A>T
AA Mutation p.Lys227Asn(p.K227N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21973187:21973187(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1847A>G
AA Mutation p.Lys616Arg(p.K616R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000397126
Start 21971972:21971972(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3062A>C
AA Mutation p.Lys1021Thr(p.K1021T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000397126
Start 21972610:21972610(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2424A>G
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000397126
Start 21974746:21974746(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.288A>G
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000397126
Start 21974529:21974529(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.505G>T
AA Mutation p.Gly169Ter(p.G169*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript