Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RHO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296271
Start	129532614:129532614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150250946
CDS Mutation	c.778G>A
AA Mutation	p.Ala260Thr(p.A260T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296271
Start	129528942:129528942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143559914
CDS Mutation	c.209C>T
AA Mutation	p.Thr70Met(p.T70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296271
Start	129533696:129533696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183318466
CDS Mutation	c.1025C>T
AA Mutation	p.Thr342Met(p.T342M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296271
Start	129529042:129529042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149615742
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296271
Start	129532320:129532320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147005807
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296271
Start	129532299:129532299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755674549
CDS Mutation	c.579G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296271
Start	129533640:129533640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142771862
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RHO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296271
Start	129528906:129528906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28933394
CDS Mutation	c.173C>T
AA Mutation	p.Thr58Met(p.T58M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296271
Start	129528780:129528780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201340914
CDS Mutation	c.47C>T
AA Mutation	p.Ala16Val(p.A16V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296271
Start	129532685:129532685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377120794
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296271
Start	129532377:129532377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657C>A
Mutation Classification	Silent
Feature Type	Transcript