Primary Site >> Stomach Cancer

Gene >> DLX5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000222598
Start 97020956:97020956(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.650C>T
AA Mutation p.Ser217Leu(p.S217L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000222598
Start 97024374:97024374(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.250G>A
AA Mutation p.Ala84Thr(p.A84T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000222598
Start 97022220:97022220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769554704
CDS Mutation c.505G>A
AA Mutation p.Glu169Lys(p.E169K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000222598
Start 97024475:97024475(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.149C>T
AA Mutation p.Pro50Leu(p.P50L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000222598
Start 97022211:97022211(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.514G>A
AA Mutation p.Ala172Thr(p.A172T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000222598
Start 97024389:97024389(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.235G>A
AA Mutation p.Gly79Ser(p.G79S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000222598
Start 97022312:97022312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413G>A
AA Mutation p.Arg138His(p.R138H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000222598
Start 97024480:97024480(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.144C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000222598
Start 97020760:97020760(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.846G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000222598
Start 97024466:97024466(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.158delG
AA Mutation p.Gly53GlufsTer28(p.G53Efs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000222598
Start 97022293:97022293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.432T>G
AA Mutation p.Tyr144Ter(p.Y144*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript