Primary Site >> Stomach Cancer

Gene >> PTAFR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000305392
Start 28150087:28150087(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.935G>A
AA Mutation p.Arg312His(p.R312H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000305392
Start 28150259:28150259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.763T>C
AA Mutation p.Trp255Arg(p.W255R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000305392
Start 28151018:28151018(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4G>A
AA Mutation p.Glu2Lys(p.E2K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000305392
Start 28150403:28150403(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.619C>A
AA Mutation p.Leu207Met(p.L207M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000305392
Start 28150621:28150621(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.401G>T
AA Mutation p.Gly134Val(p.G134V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000305392
Start 28150765:28150765(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.257C>A
AA Mutation p.Pro86His(p.P86H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000305392
Start 28150079:28150079(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.943C>T
AA Mutation p.Arg315Trp(p.R315W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000305392
Start 28150695:28150695(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.327C>T
Mutation Classification Silent
Feature Type Transcript