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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> CYP21A2
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000418967
Start
32040179:32040179(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs151344505
CDS Mutation
c.913G>A
AA Mutation
p.Val305Met(p.V305M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000418967
Start
32040722:32040722(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs770449904
CDS Mutation
c.1173C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000418967
Start
32040710:32040710(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs777369062
CDS Mutation
c.1161G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000418967
Start
32040516:32040516(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs144104274
CDS Mutation
c.1050C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000418967
Start
32038515:32038515(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.93G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000418967
Start
32040707:32040707(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1158T>C
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000418967
Start
32040453:32040453(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs763722637
CDS Mutation
c.987T>C
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000418967
Start
32040182:32040183(version: GRCh38)
Mutation Type
INS
dbSNP_RS
novel
CDS Mutation
c.916_917insC
AA Mutation
p.Val306AlafsTer8(p.V306Afs*8)
Mutation Classification
Frame_Shift_Ins
Feature Type
Transcript
Rectum Cancer: Gene >> CYP21A2
No Mutation Annotation!