Primary Site >> Stomach Cancer

Gene >> CHI3L1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000255409
Start 203183675:203183675(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745563186
CDS Mutation c.431G>A
AA Mutation p.Arg144Gln(p.R144Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000255409
Start 203181236:203181236(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147953761
CDS Mutation c.637C>T
AA Mutation p.Arg213Cys(p.R213C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000255409
Start 203181254:203181254(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141218577
CDS Mutation c.619G>A
AA Mutation p.Asp207Asn(p.D207N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000255409
Start 203179835:203179835(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148946875
CDS Mutation c.937G>A
AA Mutation p.Gly313Ser(p.G313S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000255409
Start 203183648:203183648(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.458T>C
AA Mutation p.Leu153Pro(p.L153P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000255409
Start 203179771:203179771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1001T>C
AA Mutation p.Val334Ala(p.V334A)
Mutation Classification Missense_Mutation
Feature Type Transcript