Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PHACTR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59767239:59767239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595C>T
AA Mutation	p.Pro199Ser(p.P199S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59774305:59774305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989C>T
AA Mutation	p.Thr330Met(p.T330M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59840383:59840383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1399A>C
AA Mutation	p.Thr467Pro(p.T467P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59767354:59767354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139799389
CDS Mutation	c.710C>T
AA Mutation	p.Pro237Leu(p.P237L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59841461:59841461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1513G>A
AA Mutation	p.Val505Met(p.V505M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59806153:59806153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1287A>C
AA Mutation	p.Glu429Asp(p.E429D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59773432:59773432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905C>A
AA Mutation	p.Ala302Asp(p.A302D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59845219:59845219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1618A>C
AA Mutation	p.Lys540Gln(p.K540Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59743263:59743263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762960052
CDS Mutation	c.275C>T
AA Mutation	p.Thr92Met(p.T92M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59767325:59767325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.681G>T
AA Mutation	p.Gln227His(p.Q227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59774376:59774376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060A>G
AA Mutation	p.Thr354Ala(p.T354A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59743134:59743134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143288140
CDS Mutation	c.146G>A
AA Mutation	p.Arg49His(p.R49H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59773319:59773319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755553999
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59755285:59755285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765980434
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59806078:59806078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59841505:59841505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1557A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59774381:59774381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371621892
CDS Mutation	c.1065C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59743123:59743123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780703888
CDS Mutation	c.135G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59806177:59806177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200786094
CDS Mutation	c.1311C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PHACTR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59743161:59743161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173G>A
AA Mutation	p.Arg58Gln(p.R58Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59840404:59840404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420G>A
AA Mutation	p.Glu474Lys(p.E474K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59755286:59755286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774977196
CDS Mutation	c.463G>A
AA Mutation	p.Gly155Arg(p.G155R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371015
Start	59755311:59755311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745894750
CDS Mutation	c.488A>G
AA Mutation	p.Asp163Gly(p.D163G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59774450:59774450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1134G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59806078:59806078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371015
Start	59836553:59836553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000371015
Start	59841446:59841446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>T
AA Mutation	p.Arg500Ter(p.R500*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000371015
Start	59845204:59845204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603G>T
AA Mutation	p.Glu535Ter(p.E535*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript