Primary Site >> Stomach Cancer

Gene >> TBX2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000240328
Start 61404617:61404617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769157834
CDS Mutation c.899C>T
AA Mutation p.Thr300Met(p.T300M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000240328
Start 61401940:61401940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.652A>G
AA Mutation p.Lys218Glu(p.K218E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000240328
Start 61401911:61401911(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760368587
CDS Mutation c.623A>G
AA Mutation p.Lys208Arg(p.K208R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000240328
Start 61401933:61401933(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.645C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000240328
Start 61400191:61400191(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.15G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000240328
Start 61404690:61404690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.972G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000240328
Start 61405494:61405494(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1344G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000240328
Start 61401780:61401780(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.492C>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000240328
Start 61401877:61401878(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.590dupA
AA Mutation p.Gln198AlafsTer5(p.Q198Afs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000240328
Start 61401872:61401873(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.589dupG
AA Mutation p.Glu197GlyfsTer6(p.E197Gfs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript