Colon Cancer: Gene >> WDTC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27306373:27306373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2024G>T
AA Mutation	p.Arg675Leu(p.R675L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27303746:27303746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1594G>A
AA Mutation	p.Gly532Ser(p.G532S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27297969:27297969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775108929
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Cys(p.R364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27306210:27306210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1861G>A
AA Mutation	p.Val621Met(p.V621M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27303738:27303738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1586G>A
AA Mutation	p.Arg529His(p.R529H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27303787:27303787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635C>A
AA Mutation	p.Phe545Leu(p.F545L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27301365:27301365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749589659
CDS Mutation	c.1372G>A
AA Mutation	p.Asp458Asn(p.D458N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319394
Start	27296394:27296394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319394
Start	27261087:27261087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769381504
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319394
Start	27283371:27283371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319394
Start	27294617:27294617(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769802514
CDS Mutation	c.868delG
AA Mutation	p.Glu290AsnfsTer8(p.E290Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WDTC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27305032:27305032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675G>A
AA Mutation	p.Asp559Asn(p.D559N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27283440:27283440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282C>A
AA Mutation	p.Phe94Leu(p.F94L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319394
Start	27303785:27303785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1633T>G
AA Mutation	p.Phe545Val(p.F545V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319394
Start	27283419:27283419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746581790
CDS Mutation	c.261G>A
Mutation Classification	Silent
Feature Type	Transcript