Primary Site >> Stomach Cancer

Gene >> NR2F2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394166
Start 96334174:96334174(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.541T>C
AA Mutation p.Tyr181His(p.Y181H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394166
Start 96337453:96337453(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1076G>A
AA Mutation p.Arg359Lys(p.R359K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394166
Start 96334303:96334303(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.670G>C
AA Mutation p.Val224Leu(p.V224L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000394166
Start 96334236:96334236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.603G>A
AA Mutation p.Met201Ile(p.M201I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000394166
Start 96334292:96334292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.659T>C
AA Mutation p.Leu220Pro(p.L220P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000394166
Start 96334583:96334583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.950C>T
AA Mutation p.Ala317Val(p.A317V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000394166
Start 96334272:96334272(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.639C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000394166
Start 96337550:96337550(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1173C>A
Mutation Classification Silent
Feature Type Transcript