Colon Cancer: Gene >> DDX11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31084610:31084610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421G>A
AA Mutation	p.Glu141Lys(p.E141K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31091752:31091752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123G>A
AA Mutation	p.Ala375Thr(p.A375T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31101869:31101869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748906306
CDS Mutation	c.2089G>A
AA Mutation	p.Gly697Ser(p.G697S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31093250:31093250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148220883
CDS Mutation	c.1295G>A
AA Mutation	p.Arg432His(p.R432H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31101950:31101950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2170G>T
AA Mutation	p.Gly724Cys(p.G724C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31083877:31083877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758984389
CDS Mutation	c.209G>A
AA Mutation	p.Arg70His(p.R70H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31103990:31103990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2870C>T
AA Mutation	p.Thr957Ile(p.T957I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31101033:31101033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1955T>C
AA Mutation	p.Val652Ala(p.V652A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31089060:31089060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701G>A
AA Mutation	p.Arg234Gln(p.R234Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31094787:31094787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1447T>A
AA Mutation	p.Phe483Ile(p.F483I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31085030:31085030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542G>A
AA Mutation	p.Gly181Asp(p.G181D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31101950:31101950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2170G>C
AA Mutation	p.Gly724Arg(p.G724R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000545668
Start	31096348:31096348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1490G>A
AA Mutation	p.Arg497Gln(p.R497Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545668
Start	31103979:31103979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2859G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545668
Start	31089426:31089426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545668
Start	31097985:31097985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1863T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000545668
Start	31097979:31097979(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs766120336
CDS Mutation	c.1862delG
AA Mutation	p.Gly621ValfsTer32(p.G621Vfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000545668
Start	31100634:31100634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1876-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DDX11

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545668
Start	31093308:31093308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150301253
CDS Mutation	c.1353C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545668
Start	31094801:31094801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript