Primary Site >> Stomach Cancer

Gene >> CALR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316448
Start 12940360:12940360(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.610C>T
AA Mutation p.Pro204Ser(p.P204S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000316448
Start 12940612:12940612(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773932539
CDS Mutation c.774C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000316448
Start 12943904:12943904(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148604761
CDS Mutation c.1245C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence splice_donor_variant
Transcription ID ENST00000316448
Start 12940453:12940453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.702+1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 5
Mutation Consequence inframe_deletion
Transcription ID ENST00000316448
Start 12943840:12943860(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1182_1202delTGAGGAGGATGAGGAGGACAA
AA Mutation p.Asp394_Lys401delinsGlu(p.D394_K401delinsE)
Mutation Classification In_Frame_Del
Feature Type Transcript