Primary Site >> Stomach Cancer

Gene >> CLEC7A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000304084
Start 10130022:10130022(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569206585
CDS Mutation c.61G>A
AA Mutation p.Asp21Asn(p.D21N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000304084
Start 10125410:10125410(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.379T>C
AA Mutation p.Tyr127His(p.Y127H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000304084
Start 10118526:10118526(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.676T>C
AA Mutation p.Ser226Pro(p.S226P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000304084
Start 10118523:10118523(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.679G>A
AA Mutation p.Val227Ile(p.V227I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000304084
Start 10125443:10125443(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.346C>A
AA Mutation p.Leu116Ile(p.L116I)
Mutation Classification Missense_Mutation
Feature Type Transcript