Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ACTR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263238
Start	113942342:113942342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841A>C
AA Mutation	p.Ile281Leu(p.I281L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263238
Start	113942309:113942309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760969306
CDS Mutation	c.808G>A
AA Mutation	p.Asp270Asn(p.D270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263238
Start	113951543:113951543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923C>A
AA Mutation	p.Pro308His(p.P308H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263238
Start	113940075:113940075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657A>C
AA Mutation	p.Gln219His(p.Q219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263238
Start	113951767:113951767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263238
Start	113939979:113939979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACTR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263238
Start	113942189:113942189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200071930
CDS Mutation	c.688C>T
AA Mutation	p.Arg230Cys(p.R230C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263238
Start	113957389:113957389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1191A>C
AA Mutation	p.Lys397Asn(p.K397N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263238
Start	113940000:113940000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582A>G
Mutation Classification	Silent
Feature Type	Transcript