Primary Site >> Stomach Cancer

Gene >> DMTN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265800
Start 22070295:22070295(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.565A>G
AA Mutation p.Thr189Ala(p.T189A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265800
Start 22073799:22073799(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.799A>C
AA Mutation p.Thr267Pro(p.T267P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265800
Start 22081428:22081428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1183C>T
AA Mutation p.Arg395Trp(p.R395W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265800
Start 22070326:22070326(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.596C>T
AA Mutation p.Ala199Val(p.A199V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265800
Start 22069041:22069041(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377647942
CDS Mutation c.275C>T
AA Mutation p.Ser92Phe(p.S92F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000265800
Start 22081421:22081421(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1176G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000265800
Start 22069041:22069041(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.281delC
AA Mutation p.Pro94HisfsTer137(p.P94Hfs*137)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000265800
Start 22069483:22069483(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.364delC
AA Mutation p.Arg122GlyfsTer109(p.R122Gfs*109)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000265800
Start 22070312:22070312(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.587delC
AA Mutation p.Pro196ArgfsTer35(p.P196Rfs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript