Primary Site >> Stomach Cancer

Gene >> PAQR3

ID 1
Mutation Consequence missense_variant;NMD_transcript_variant
Transcription ID ENST00000511594
Start 78923885:78923885(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.765T>G
AA Mutation p.Ile255Met(p.I255M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;NMD_transcript_variant
Transcription ID ENST00000511594
Start 78920623:78920623(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.852G>A
AA Mutation p.Met284Ile(p.M284I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;NMD_transcript_variant
Transcription ID ENST00000511594
Start 78923940:78923940(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375034424
CDS Mutation c.710C>T
AA Mutation p.Ala237Val(p.A237V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;NMD_transcript_variant
Transcription ID ENST00000511594
Start 78920633:78920633(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.842C>T
AA Mutation p.Ala281Val(p.A281V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant;NMD_transcript_variant
Transcription ID ENST00000511594
Start 78935169:78935169(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs190190715
CDS Mutation c.300G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant;NMD_transcript_variant
Transcription ID ENST00000511594
Start 78920578:78920578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.897A>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained;NMD_transcript_variant
Transcription ID ENST00000511594
Start 78939166:78939166(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.59G>A
AA Mutation p.Trp20Ter(p.W20*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript