Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CALR

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000316448
Start 12939235:12939235(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.193G>T
AA Mutation p.Gly65Cys(p.G65C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316448
Start 12940417:12940417(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.667G>A
AA Mutation p.Ala223Thr(p.A223T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316448
Start 12943890:12943890(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746740154
CDS Mutation c.1231G>A
AA Mutation p.Gly411Ser(p.G411S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316448
Start 12939542:12939542(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.308T>C
AA Mutation p.Ile103Thr(p.I103T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000316448
Start 12939552:12939552(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.318G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000316448
Start 12943620:12943620(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747325385
CDS Mutation c.1044C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000316448
Start 12940117:12940117(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143361476
CDS Mutation c.462C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000316448
Start 12940625:12940625(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.791delC
AA Mutation p.Pro264GlnfsTer2(p.P264Qfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> CALR

No Mutation Annotation!