Colon Cancer: Gene >> FZD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103329999:103329999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886C>T
AA Mutation	p.Ser629Phe(p.S629F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103318657:103318657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245T>C
AA Mutation	p.Val82Ala(p.V82A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103329990:103329990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1877C>G
AA Mutation	p.Ser626Cys(p.S626C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103318608:103318608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.196A>C
AA Mutation	p.Asn66His(p.N66H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103324489:103324489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383A>G
AA Mutation	p.Tyr128Cys(p.Y128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103331369:103331369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1981A>G
AA Mutation	p.Thr661Ala(p.T661A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103325041:103325041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.935G>T
AA Mutation	p.Gly312Val(p.G312V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103328401:103328401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143405641
CDS Mutation	c.1526G>A
AA Mutation	p.Arg509Gln(p.R509Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103330004:103330004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1891G>A
AA Mutation	p.Glu631Lys(p.E631K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103318698:103318698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358755
Start	103328336:103328336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358755
Start	103324499:103324499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358755
Start	103300228:103300228(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.125delT
AA Mutation	p.Phe42SerfsTer4(p.F42Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000358755
Start	103328358:103328358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483G>T
AA Mutation	p.Gly495Ter(p.G495*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000358755
Start	103318738:103318738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326T>G
AA Mutation	p.Leu109Ter(p.L109*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000358755
Start	103328418:103328418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1541+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FZD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103325339:103325339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233G>T
AA Mutation	p.Lys411Asn(p.K411N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103324572:103324572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466G>T
AA Mutation	p.Asp156Tyr(p.D156Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103324780:103324780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674G>A
AA Mutation	p.Arg225Lys(p.R225K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript