Colon Cancer: Gene >> SON

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33552499:33552499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3268C>T
AA Mutation	p.Arg1090Trp(p.R1090W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33575795:33575795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7123G>A
AA Mutation	p.Ala2375Thr(p.A2375T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33554816:33554816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758958383
CDS Mutation	c.5585G>A
AA Mutation	p.Arg1862His(p.R1862H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33554282:33554282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200562903
CDS Mutation	c.5051C>A
AA Mutation	p.Pro1684His(p.P1684H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33550859:33550859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755601747
CDS Mutation	c.1628C>T
AA Mutation	p.Thr543Met(p.T543M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33550963:33550963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1732G>A
AA Mutation	p.Ala578Thr(p.A578T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33552596:33552596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752556728
CDS Mutation	c.3365G>A
AA Mutation	p.Arg1122His(p.R1122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33551257:33551257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2026C>T
AA Mutation	p.Pro676Ser(p.P676S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33559245:33559245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6337G>A
AA Mutation	p.Ala2113Thr(p.A2113T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33553753:33553753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4522C>T
AA Mutation	p.His1508Tyr(p.H1508Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33552107:33552107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2876C>T
AA Mutation	p.Thr959Ile(p.T959I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33549853:33549853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>A
AA Mutation	p.Ala208Thr(p.A208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33553852:33553852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4621A>G
AA Mutation	p.Ile1541Val(p.I1541V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33575839:33575839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7167A>C
AA Mutation	p.Glu2389Asp(p.E2389D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33552959:33552959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3728A>C
AA Mutation	p.Glu1243Ala(p.E1243A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33555341:33555341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6110G>T
AA Mutation	p.Arg2037Ile(p.R2037I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33551837:33551837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2606G>A
AA Mutation	p.Gly869Asp(p.G869D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33553774:33553774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4543G>T
AA Mutation	p.Ala1515Ser(p.A1515S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33552717:33552717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3486T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33550860:33550860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1629G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33550134:33550134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.903G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33549507:33549507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33551235:33551235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757329300
CDS Mutation	c.2004C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33549651:33549651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763843570
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33554439:33554439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760341788
CDS Mutation	c.5208G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33550873:33550873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SON

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33554700:33554700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5469A>T
AA Mutation	p.Arg1823Ser(p.R1823S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33555287:33555287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6056G>A
AA Mutation	p.Arg2019Gln(p.R2019Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33552271:33552271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3040G>A
AA Mutation	p.Glu1014Lys(p.E1014K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33553951:33553951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4720C>G
AA Mutation	p.Gln1574Glu(p.Q1574E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33549609:33549609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378A>C
AA Mutation	p.Glu126Asp(p.E126D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33553524:33553524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4293G>T
AA Mutation	p.Met1431Ile(p.M1431I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33555341:33555341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6110G>T
AA Mutation	p.Arg2037Ile(p.R2037I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33557270:33557270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6275A>G
AA Mutation	p.Lys2092Arg(p.K2092R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356577
Start	33554384:33554384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5153A>G
AA Mutation	p.Asp1718Gly(p.D1718G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356577
Start	33550860:33550860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367848437
CDS Mutation	c.1629G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000356577
Start	33559229:33559229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6322-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript