Colon Cancer: Gene >> WNT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225512
Start	46768760:46768760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628G>A
AA Mutation	p.Gly210Arg(p.G210R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225512
Start	46769842:46769842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>A
AA Mutation	p.Glu177Lys(p.E177K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225512
Start	46769820:46769820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551C>T
AA Mutation	p.Ser184Leu(p.S184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225512
Start	46768496:46768496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Trp(p.R298W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225512
Start	46768472:46768472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757727243
CDS Mutation	c.916G>A
AA Mutation	p.Gly306Ser(p.G306S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000225512
Start	46818578:46818578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20G>T
AA Mutation	p.Gly7Val(p.G7V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225512
Start	46768659:46768659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000225512
Start	46773666:46773666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WNT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225512
Start	46768426:46768426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962C>T
AA Mutation	p.Thr321Met(p.T321M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225512
Start	46769855:46769855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225512
Start	46773801:46773801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript