Primary Site >> Stomach Cancer

Gene >> TFAP2A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000482890
Start 10414951:10414951(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.35A>C
AA Mutation p.Glu12Ala(p.E12A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000482890
Start 10398538:10398538(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1193T>C
AA Mutation p.Leu398Pro(p.L398P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000482890
Start 10410262:10410262(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.119C>T
AA Mutation p.Thr40Met(p.T40M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000482890
Start 10402547:10402547(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.828G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000482890
Start 10398639:10398639(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1092C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000482890
Start 10402571:10402571(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.804delA
AA Mutation p.Lys268AsnfsTer5(p.K268Nfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000482890
Start 10402596:10402596(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.779delA
AA Mutation p.Asn260MetfsTer6(p.N260Mfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript