Colon Cancer: Gene >> CDC23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138189845:138189845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486G>T
AA Mutation	p.Asp496Tyr(p.D496Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138206617:138206617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302G>T
AA Mutation	p.Arg101Leu(p.R101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394886
Start	138202115:138202115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413T>C
AA Mutation	p.Leu138Ser(p.L138S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138192284:138192284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369097703
CDS Mutation	c.1271G>A
AA Mutation	p.Arg424Gln(p.R424Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138189025:138189025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1747C>A
AA Mutation	p.Pro583Thr(p.P583T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138191888:138191888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1336C>G
AA Mutation	p.Leu446Val(p.L446V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138191923:138191923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301G>A
AA Mutation	p.Arg434His(p.R434H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138192639:138192639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767536014
CDS Mutation	c.1031G>A
AA Mutation	p.Arg344His(p.R344H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138198273:138198273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938A>C
AA Mutation	p.Lys313Thr(p.K313T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138192316:138192316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239G>T
AA Mutation	p.Lys413Asn(p.K413N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138192614:138192614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056A>C
AA Mutation	p.Leu352Phe(p.L352F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138201415:138201415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374640902
CDS Mutation	c.449C>T
AA Mutation	p.Ala150Val(p.A150V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000394886
Start	138191514:138191514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761053901
CDS Mutation	c.1384G>A
AA Mutation	p.Val462Met(p.V462M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394886
Start	138198648:138198648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394886
Start	138206568:138206568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394886
Start	138198737:138198738(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.699dupT
AA Mutation	p.Leu234SerfsTer23(p.L234Sfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000394886
Start	138192502:138192502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CDC23

No Mutation Annotation!