Primary Site >> Stomach Cancer

Gene >> IFNA17

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000413767
Start 21228094:21228094(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.80C>A
AA Mutation p.Pro27His(p.P27H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000413767
Start 21227954:21227954(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150705157
CDS Mutation c.220A>G
AA Mutation p.Thr74Ala(p.T74A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000413767
Start 21227939:21227939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.235G>A
AA Mutation p.Val79Ile(p.V79I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000413767
Start 21227999:21227999(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745361920
CDS Mutation c.175T>A
AA Mutation p.Phe59Ile(p.F59I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000413767
Start 21227999:21227999(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.175T>C
AA Mutation p.Phe59Leu(p.F59L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000413767
Start 21227978:21227978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.196T>C
AA Mutation p.Phe66Leu(p.F66L)
Mutation Classification Missense_Mutation
Feature Type Transcript