Primary Site >> Stomach Cancer

Gene >> TMEFF2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000272771
Start 191953779:191953779(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763546804
CDS Mutation c.928G>A
AA Mutation p.Val310Ile(p.V310I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000272771
Start 192057712:192057712(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.503G>A
AA Mutation p.Gly168Asp(p.G168D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000272771
Start 192184416:192184416(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774382007
CDS Mutation c.350G>A
AA Mutation p.Arg117Gln(p.R117Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000272771
Start 192194424:192194424(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376482759
CDS Mutation c.101G>A
AA Mutation p.Arg34His(p.R34H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000272771
Start 192194477:192194477(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372412462
CDS Mutation c.48C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000272771
Start 192194369:192194369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.156C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000272771
Start 191999169:191999170(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.575dupA
AA Mutation p.Asn192LysfsTer7(p.N192Kfs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript