Primary Site >> Stomach Cancer

Gene >> PHF19

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000373896
Start 120874605:120874605(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.137T>C
AA Mutation p.Val46Ala(p.V46A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000373896
Start 120858045:120858045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1642C>T
AA Mutation p.Arg548Trp(p.R548W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000373896
Start 120862621:120862621(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1097C>T
AA Mutation p.Ser366Phe(p.S366F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000373896
Start 120862612:120862612(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150134029
CDS Mutation c.1106G>A
AA Mutation p.Arg369His(p.R369H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000373896
Start 120874571:120874571(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757442570
CDS Mutation c.171C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000373896
Start 120858094:120858094(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1593C>A
Mutation Classification Silent
Feature Type Transcript