Primary Site >> Stomach Cancer

Gene >> TFDP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375370
Start 113637827:113637827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1016A>G
AA Mutation p.Gln339Arg(p.Q339R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375370
Start 113633187:113633187(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.376A>G
AA Mutation p.Lys126Glu(p.K126E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375370
Start 113636035:113636035(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747551137
CDS Mutation c.746G>A
AA Mutation p.Arg249Gln(p.R249Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375370
Start 113611032:113611032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.49T>A
AA Mutation p.Phe17Ile(p.F17I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000375370
Start 113611055:113611055(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144432965
CDS Mutation c.72C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000375370
Start 113633235:113633235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.424C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000375370
Start 113633901:113633902(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.491dupA
AA Mutation p.Asn164LysfsTer51(p.N164Kfs*51)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript