Primary Site >> Stomach Cancer

Gene >> IL4R

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395762
Start 27363054:27363054(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749041212
CDS Mutation c.1702G>A
AA Mutation p.Val568Ile(p.V568I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395762
Start 27352558:27352558(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.532A>G
AA Mutation p.Thr178Ala(p.T178A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395762
Start 27346611:27346611(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145473866
CDS Mutation c.506C>T
AA Mutation p.Pro169Leu(p.P169L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395762
Start 27363559:27363559(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2207C>T
AA Mutation p.Thr736Ile(p.T736I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395762
Start 27362916:27362916(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1564C>T
AA Mutation p.His522Tyr(p.H522Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000395762
Start 27358963:27358963(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766606481
CDS Mutation c.818G>A
AA Mutation p.Arg273His(p.R273H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000395762
Start 27362801:27362801(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1449T>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000395762
Start 27342135:27342135(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000395762
Start 27363107:27363107(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1755T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000395762
Start 27355814:27355814(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.679delG
AA Mutation p.Glu227SerfsTer51(p.E227Sfs*51)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000395762
Start 27363398:27363398(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2050delG
AA Mutation p.Glu684LysfsTer3(p.E684Kfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript