Primary Site >> Stomach Cancer

Gene >> SOX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000330949
Start 112068029:112068029(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.371G>A
AA Mutation p.Arg124His(p.R124H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000330949
Start 112067938:112067938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.280G>A
AA Mutation p.Glu94Lys(p.E94K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000330949
Start 112068041:112068041(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.383C>T
AA Mutation p.Thr128Met(p.T128M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000330949
Start 112067962:112067962(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.304G>A
AA Mutation p.Asp102Asn(p.D102N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000330949
Start 112067858:112067858(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.200G>A
AA Mutation p.Arg67His(p.R67H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000330949
Start 112067980:112067980(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.322C>T
AA Mutation p.Arg108Cys(p.R108C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000330949
Start 112067982:112067982(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.324C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000330949
Start 112067976:112067976(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.318G>A
Mutation Classification Silent
Feature Type Transcript