Colon Cancer: Gene >> FZD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28520818:28520818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>T
AA Mutation	p.Asp124Tyr(p.D124Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28562892:28562892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200915090
CDS Mutation	c.1882C>T
AA Mutation	p.Arg628Trp(p.R628W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28527270:28527270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510A>C
AA Mutation	p.Lys170Asn(p.K170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28527173:28527173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413C>A
AA Mutation	p.Pro138His(p.P138H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28527791:28527791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1031T>C
AA Mutation	p.Ile344Thr(p.I344T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28555961:28555961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1777C>T
AA Mutation	p.Arg593Cys(p.R593C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28527914:28527914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154T>C
AA Mutation	p.Val385Ala(p.V385A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28555938:28555938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1754A>G
AA Mutation	p.Tyr585Cys(p.Y585C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240093
Start	28527615:28527615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.855C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000240093
Start	28551725:28551725(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1533delT
AA Mutation	p.His512MetfsTer8(p.H512Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000240093
Start	28527641:28527642(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs765036679
CDS Mutation	c.888dupT
AA Mutation	p.Thr297TyrfsTer25(p.T297Yfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FZD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28527542:28527542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750699469
CDS Mutation	c.782G>A
AA Mutation	p.Arg261Gln(p.R261Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28520704:28520704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256G>A
AA Mutation	p.Ala86Thr(p.A86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28503125:28503125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112G>T
AA Mutation	p.Asp38Tyr(p.D38Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000240093
Start	28527859:28527859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372290611
CDS Mutation	c.1099G>A
AA Mutation	p.Asp367Asn(p.D367N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240093
Start	28527573:28527573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769967376
CDS Mutation	c.813A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000240093
Start	28527961:28527961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201C>T
AA Mutation	p.Arg401Ter(p.R401*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript