Colon Cancer: Gene >> CSF2RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1288831:1288831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777638014
CDS Mutation	c.416C>T
AA Mutation	p.Ala139Val(p.A139V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1288589:1288589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290A>G
AA Mutation	p.His97Arg(p.H97R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1288538:1288538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239C>T
AA Mutation	p.Ser80Leu(p.S80L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1288591:1288591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767686310
CDS Mutation	c.292G>A
AA Mutation	p.Val98Met(p.V98M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1290468:1290468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605G>A
AA Mutation	p.Gly202Asp(p.G202D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1294424:1294424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743A>G
AA Mutation	p.Tyr248Cys(p.Y248C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1290477:1290477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614T>A
AA Mutation	p.Phe205Tyr(p.F205Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1288807:1288807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762479130
CDS Mutation	c.392C>T
AA Mutation	p.Ala131Val(p.A131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1285810:1285810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775556939
CDS Mutation	c.109A>G
AA Mutation	p.Asn37Asp(p.N37D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381524
Start	1288808:1288808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143104828
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381524
Start	1288844:1288844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368476257
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381524
Start	1303933:1303933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752209055
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381524
Start	1295453:1295453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000381524
Start	1295426:1295426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CSF2RA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381524
Start	1282777:1282777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757087323
CDS Mutation	c.74C>T
AA Mutation	p.Ser25Leu(p.S25L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1288549:1288549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758063598
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Cys(p.R84C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381524
Start	1309445:1309445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749182596
CDS Mutation	c.1169G>A
AA Mutation	p.Arg390His(p.R390H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381524
Start	1288844:1288844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368476257
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript