Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CSF3R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36472663:36472663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150616658
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Trp(p.R233W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36475450:36475450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288G>T
AA Mutation	p.Gln96His(p.Q96H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36467879:36467879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765606679
CDS Mutation	c.1807G>T
AA Mutation	p.Ala603Ser(p.A603S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36475524:36475524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375879178
CDS Mutation	c.214G>A
AA Mutation	p.Gly72Arg(p.G72R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36473485:36473485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372288734
CDS Mutation	c.623C>T
AA Mutation	p.Ala208Val(p.A208V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36472606:36472606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754T>C
AA Mutation	p.Cys252Arg(p.C252R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36468195:36468195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1603C>A
AA Mutation	p.Leu535Ile(p.L535I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36469805:36469805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321G>T
AA Mutation	p.Asp441Tyr(p.D441Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36466595:36466595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2273G>T
AA Mutation	p.Ser758Ile(p.S758I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36466624:36466624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2244T>G
AA Mutation	p.Asp748Glu(p.D748E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36466751:36466751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776535279
CDS Mutation	c.2117C>T
AA Mutation	p.Pro706Leu(p.P706L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36472555:36472555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805C>T
AA Mutation	p.Arg269Cys(p.R269C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36472651:36472651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709C>A
AA Mutation	p.Pro237Thr(p.P237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36467287:36467287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1983T>A
AA Mutation	p.Ser661Arg(p.S661R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361632
Start	36466627:36466627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372773604
CDS Mutation	c.2241C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361632
Start	36468106:36468106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1692C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361632
Start	36471566:36471566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361632
Start	36469722:36469722(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769210858
CDS Mutation	c.1404delC
AA Mutation	p.Ser469AlafsTer22(p.S469Afs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CSF3R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36475470:36475470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268C>T
AA Mutation	p.Pro90Ser(p.P90S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36473879:36473879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370G>T
AA Mutation	p.Ala124Ser(p.A124S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361632
Start	36468209:36468209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589C>T
AA Mutation	p.Ala530Val(p.A530V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361632
Start	36469820:36469820(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1306delC
AA Mutation	p.His436MetfsTer12(p.H436Mfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000361632
Start	36467566:36467566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1950C>A
AA Mutation	p.Cys650Ter(p.C650*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript