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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
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!