Primary Site >> Stomach Cancer

Gene >> DLX2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000234198
Start 172100817:172100817(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.713C>T
AA Mutation p.Pro238Leu(p.P238L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000234198
Start 172101584:172101584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.463C>A
AA Mutation p.Pro155Thr(p.P155T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000234198
Start 172100560:172100560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.970G>A
AA Mutation p.Ala324Thr(p.A324T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000234198
Start 172101580:172101580(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.467G>A
AA Mutation p.Arg156His(p.R156H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000234198
Start 172100582:172100582(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.948C>T
Mutation Classification Silent
Feature Type Transcript