Primary Site >> Stomach Cancer

Gene >> CDR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370532
Start 140784010:140784010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.357A>C
AA Mutation p.Glu119Asp(p.E119D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370532
Start 140784282:140784282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85G>A
AA Mutation p.Glu29Lys(p.E29K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370532
Start 140783653:140783653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.714T>G
AA Mutation p.Ile238Met(p.I238M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370532
Start 140784057:140784057(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.310G>A
AA Mutation p.Asp104Asn(p.D104N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000370532
Start 140783635:140783635(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.732G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000370532
Start 140783896:140783896(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.471C>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000370532
Start 140783755:140783755(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.612G>A
Mutation Classification Silent
Feature Type Transcript