Colon Cancer: Gene >> CDC45

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19505434:19505434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777G>T
AA Mutation	p.Glu259Asp(p.E259D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19497437:19497437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>A
AA Mutation	p.Asp215Asn(p.D215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19483871:19483871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352C>T
AA Mutation	p.Leu118Phe(p.L118F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19507489:19507489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144918738
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Trp(p.R310W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19505450:19505450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551487753
CDS Mutation	c.793G>A
AA Mutation	p.Val265Met(p.V265M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19516602:19516602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs12158840
CDS Mutation	c.1516G>A
AA Mutation	p.Val506Met(p.V506M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263201
Start	19516640:19516640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263201
Start	19516601:19516601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776682487
CDS Mutation	c.1515C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263201
Start	19499110:19499110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263201
Start	19508596:19508596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184840047
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263201
Start	19482782:19482782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11912776
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000263201
Start	19516818:19516818(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1566delT
AA Mutation	p.Phe522LeufsTer25(p.F522Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263201
Start	19481001:19481001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.162delG
AA Mutation	p.Trp55GlyfsTer21(p.W55Gfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDC45

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19482705:19482705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220C>A
AA Mutation	p.Leu74Ile(p.L74I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19505421:19505421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541752640
CDS Mutation	c.764G>A
AA Mutation	p.Arg255Gln(p.R255Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263201
Start	19479998:19479998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.30C>A
AA Mutation	p.Phe10Leu(p.F10L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript