Primary Site >> Stomach Cancer

Gene >> CDC37

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000222005
Start 10393378:10393378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.790C>T
AA Mutation p.Arg264Trp(p.R264W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000222005
Start 10396019:10396019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.287G>A
AA Mutation p.Arg96Gln(p.R96Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000222005
Start 10396200:10396200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.106C>T
AA Mutation p.Arg36Trp(p.R36W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000222005
Start 10393321:10393321(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143134175
CDS Mutation c.847C>T
AA Mutation p.Arg283Cys(p.R283C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000222005
Start 10393301:10393301(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.867C>T
Mutation Classification Silent
Feature Type Transcript