Primary Site >> Stomach Cancer

Gene >> TCF21

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000237316
Start 133889669:133889669(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 2
Mutation Consequence missense_variant
Transcription ID ENST00000237316
Start 133889827:133889827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.430T>C
AA Mutation p.Tyr144His(p.Y144H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000237316
Start 133889619:133889619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.222G>T
AA Mutation p.Gln74His(p.Q74H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000237316
Start 133889560:133889560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.163G>A
AA Mutation p.Gly55Ser(p.G55S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000237316
Start 133889631:133889631(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.234G>T
AA Mutation p.Gln78His(p.Q78H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000237316
Start 133889407:133889407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10G>A
AA Mutation p.Gly4Ser(p.G4S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000237316
Start 133889583:133889583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.186G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000237316
Start 133889688:133889688(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.292delG
AA Mutation p.Ala98ProfsTer34(p.A98Pfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000237316
Start 133889674:133889674(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.277C>T
AA Mutation p.Arg93Ter(p.R93*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript