Colon Cancer: Gene >> CDK13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40094199:40094199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150957134
CDS Mutation	c.3758G>A
AA Mutation	p.Arg1253Gln(p.R1253Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40094966:40094966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4525G>A
AA Mutation	p.Gly1509Arg(p.G1509R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40045938:40045938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2456G>C
AA Mutation	p.Arg819Thr(p.R819T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40094186:40094186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3745C>G
AA Mutation	p.Pro1249Ala(p.P1249A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40045942:40045942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2460G>T
AA Mutation	p.Gln820His(p.Q820H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40062924:40062924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2699G>A
AA Mutation	p.Cys900Tyr(p.C900Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40093178:40093178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781777435
CDS Mutation	c.3629C>T
AA Mutation	p.Ser1210Leu(p.S1210L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40001887:40001887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2209C>T
AA Mutation	p.Arg737Cys(p.R737C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40088322:40088322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3226G>A
AA Mutation	p.Val1076Met(p.V1076M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	39997626:39997626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004G>T
AA Mutation	p.Lys668Asn(p.K668N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40092830:40092830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3281T>A
AA Mutation	p.Ile1094Asn(p.I1094N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40092925:40092925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3376C>A
AA Mutation	p.Leu1126Ile(p.L1126I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40045975:40045975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2493G>T
AA Mutation	p.Lys831Asn(p.K831N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40062864:40062864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761752355
CDS Mutation	c.2639G>A
AA Mutation	p.Arg880His(p.R880H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000181839
Start	40094272:40094272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3831T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000181839
Start	40093167:40093167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3618G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000181839
Start	40001877:40001877(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780713745
CDS Mutation	c.2205delA
AA Mutation	p.Val736TyrfsTer32(p.V736Yfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000181839
Start	40063048:40063048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2733delA
AA Mutation	p.Lys911AsnfsTer13(p.K911Nfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000181839
Start	39951118:39951118(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.484delG
AA Mutation	p.Ala162ProfsTer174(p.A162Pfs*174)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDK13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40094535:40094535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4094G>A
AA Mutation	p.Arg1365Gln(p.R1365Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40094949:40094949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4508G>C
AA Mutation	p.Gly1503Ala(p.G1503A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40094542:40094542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4101T>A
AA Mutation	p.Ser1367Arg(p.S1367R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	40094381:40094381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3940G>T
AA Mutation	p.Asp1314Tyr(p.D1314Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000181839
Start	39997626:39997626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004G>T
AA Mutation	p.Lys668Asn(p.K668N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript