Colon Cancer: Gene >> FZD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344575
Start	73435265:73435265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258G>A
AA Mutation	p.Gly420Ser(p.G420S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344575
Start	73435442:73435442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Trp(p.R479W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344575
Start	73435397:73435397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390G>A
AA Mutation	p.Val464Ile(p.V464I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344575
Start	73435029:73435029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1022C>T
AA Mutation	p.Ala341Val(p.A341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344575
Start	73434683:73434683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Cys(p.R226C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344575
Start	73435724:73435724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782644101
CDS Mutation	c.1717A>G
AA Mutation	p.Thr573Ala(p.T573A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344575
Start	73434868:73434868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782026570
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344575
Start	73435480:73435480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782393554
CDS Mutation	c.1473C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344575
Start	73434907:73434907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782382695
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344575
Start	73434991:73434991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FZD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344575
Start	73434779:73434779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.772C>A
AA Mutation	p.His258Asn(p.H258N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344575
Start	73434368:73434368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Cys(p.R121C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344575
Start	73435656:73435656(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1651delC
AA Mutation	p.Arg551GlyfsTer28(p.R551Gfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript