Primary Site >> Stomach Cancer

Gene >> PRDM4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000228437
Start 107734518:107734518(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747069656
CDS Mutation c.2098C>T
AA Mutation p.Arg700Cys(p.R700C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000228437
Start 107740970:107740970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1900C>T
AA Mutation p.Arg634Trp(p.R634W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000228437
Start 107754000:107754000(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.255A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000228437
Start 107734462:107734462(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2154G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000228437
Start 107754030:107754030(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.225T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000228437
Start 107752019:107752019(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.522T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000228437
Start 107752090:107752090(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.451C>T
AA Mutation p.Gln151Ter(p.Q151*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript