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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> SHC2
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000264554
Start
422406:422406(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs746427249
CDS Mutation
c.1360G>A
AA Mutation
p.Val454Met(p.V454M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000264554
Start
434779:434779(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs528045997
CDS Mutation
c.1040C>T
AA Mutation
p.Pro347Leu(p.P347L)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000264554
Start
425142:425142(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1264G>A
AA Mutation
p.Ala422Thr(p.A422T)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
missense_variant
Transcription ID
ENST00000264554
Start
422187:422187(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs779103557
CDS Mutation
c.1579G>A
AA Mutation
p.Gly527Arg(p.G527R)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
missense_variant
Transcription ID
ENST00000264554
Start
425211:425211(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs530845691
CDS Mutation
c.1195G>A
AA Mutation
p.Val399Met(p.V399M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
missense_variant
Transcription ID
ENST00000264554
Start
440893:440893(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.508C>A
AA Mutation
p.Leu170Met(p.L170M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
missense_variant
Transcription ID
ENST00000264554
Start
419011:419011(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs761490164
CDS Mutation
c.1666G>A
AA Mutation
p.Asp556Asn(p.D556N)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Rectum Cancer: Gene >> SHC2
No Mutation Annotation!