Primary Site >> Stomach Cancer

Gene >> FOXE1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375123
Start 97854405:97854405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.491C>T
AA Mutation p.Ala164Val(p.A164V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375123
Start 97854185:97854185(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768174425
CDS Mutation c.271C>T
AA Mutation p.Arg91Cys(p.R91C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375123
Start 97854351:97854351(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.437G>A
AA Mutation p.Arg146His(p.R146H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375123
Start 97854279:97854279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.365G>A
AA Mutation p.Gly122Asp(p.G122D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000375123
Start 97854344:97854344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.430C>T
AA Mutation p.Arg144Cys(p.R144C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000375123
Start 97854905:97854905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.991G>A
AA Mutation p.Gly331Ser(p.G331S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000375123
Start 97854186:97854186(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.272G>A
AA Mutation p.Arg91His(p.R91H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000375123
Start 97854995:97854995(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1081G>A
AA Mutation p.Ala361Thr(p.A361T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000375123
Start 97854298:97854298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.384G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000375123
Start 97854388:97854388(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.474G>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000375123
Start 97854970:97854970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1056C>T
Mutation Classification Silent
Feature Type Transcript