Colon Cancer: Gene >> CSF2RB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36923279:36923279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778626873
CDS Mutation	c.112G>A
AA Mutation	p.Asp38Asn(p.D38N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36929528:36929528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518T>C
AA Mutation	p.Val173Ala(p.V173A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36923336:36923336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368852888
CDS Mutation	c.169G>A
AA Mutation	p.Val57Ile(p.V57I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000403662
Start	36923366:36923366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>C
AA Mutation	p.Glu67Gln(p.E67Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36926150:36926150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202034054
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Trp(p.R122W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36933988:36933988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776366819
CDS Mutation	c.1309G>A
AA Mutation	p.Glu437Lys(p.E437K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36932848:36932848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146404001
CDS Mutation	c.1096G>A
AA Mutation	p.Glu366Lys(p.E366K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36923342:36923342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770407372
CDS Mutation	c.175G>A
AA Mutation	p.Val59Met(p.V59M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36926067:36926067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.281G>T
AA Mutation	p.Arg94Met(p.R94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36938239:36938239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144413438
CDS Mutation	c.2431G>A
AA Mutation	p.Glu811Lys(p.E811K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36937985:36937985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574382286
CDS Mutation	c.2177C>T
AA Mutation	p.Ser726Leu(p.S726L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403662
Start	36929674:36929674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.585C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403662
Start	36937764:36937764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1956G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403662
Start	36923266:36923266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000403662
Start	36937788:36937788(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1984delG
AA Mutation	p.Ala662LeufsTer36(p.A662Lfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000403662
Start	36937504:36937504(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757082963
CDS Mutation	c.1701delC
AA Mutation	p.Ser568AlafsTer130(p.S568Afs*130)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CSF2RB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000403662
Start	36932848:36932848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146404001
CDS Mutation	c.1096G>A
AA Mutation	p.Glu366Lys(p.E366K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403662
Start	36922255:36922255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765741610
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403662
Start	36932892:36932892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780806811
CDS Mutation	c.1140G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403662
Start	36930766:36930766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555140256
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript