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Mutation
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Colon Cancer: Gene >> CABLES1
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000256925
Start
23136580:23136580(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.818G>T
AA Mutation
p.Ser273Ile(p.S273I)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000256925
Start
23188896:23188896(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.904G>A
AA Mutation
p.Ala302Thr(p.A302T)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant;splice_region_variant
Transcription ID
ENST00000256925
Start
23188839:23188839(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs529420681
CDS Mutation
c.847C>T
AA Mutation
p.Arg283Trp(p.R283W)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
missense_variant
Transcription ID
ENST00000256925
Start
23253743:23253743(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.1568T>C
AA Mutation
p.Met523Thr(p.M523T)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
missense_variant
Transcription ID
ENST00000256925
Start
23253814:23253814(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.1639A>C
AA Mutation
p.Lys547Gln(p.K547Q)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
missense_variant
Transcription ID
ENST00000256925
Start
23235947:23235947(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.1238G>T
AA Mutation
p.Arg413Ile(p.R413I)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000256925
Start
23253819:23253819(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs367970943
CDS Mutation
c.1644C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000256925
Start
23253880:23253880(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1705T>C
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
9
Mutation Consequence
stop_gained
Transcription ID
ENST00000256925
Start
23194468:23194468(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.938C>G
AA Mutation
p.Ser313Ter(p.S313*)
Mutation Classification
Nonsense_Mutation
Feature Type
Transcript
Mutation ID
10
Mutation Consequence
stop_gained
Transcription ID
ENST00000256925
Start
23235979:23235979(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1270C>T
AA Mutation
p.Gln424Ter(p.Q424*)
Mutation Classification
Nonsense_Mutation
Feature Type
Transcript
Rectum Cancer: Gene >> CABLES1
No Mutation Annotation!