Colon Cancer: Gene >> FZD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44559115:44559115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1427T>C
AA Mutation	p.Val476Ala(p.V476A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44559369:44559369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148517314
CDS Mutation	c.1681G>A
AA Mutation	p.Gly561Ser(p.G561S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44559012:44559012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324C>T
AA Mutation	p.Arg442Cys(p.R442C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44558889:44558889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201G>A
AA Mutation	p.Val401Met(p.V401M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44558823:44558823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746685961
CDS Mutation	c.1135G>A
AA Mutation	p.Val379Met(p.V379M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44559223:44559223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535C>T
AA Mutation	p.Pro512Leu(p.P512L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44558898:44558898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210G>A
AA Mutation	p.Val404Ile(p.V404I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44559033:44559033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1345G>A
AA Mutation	p.Gly449Ser(p.G449S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44558577:44558577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889G>A
AA Mutation	p.Gly297Ser(p.G297S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44558952:44558952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264G>A
AA Mutation	p.Val422Met(p.V422M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44559069:44559069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381C>T
AA Mutation	p.Arg461Cys(p.R461C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44558827:44558827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139C>T
AA Mutation	p.Pro380Leu(p.P380L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44558779:44558779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091C>A
AA Mutation	p.Ala364Asp(p.A364D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000315323
Start	44558919:44558919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231C>A
AA Mutation	p.Pro411Thr(p.P411T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315323
Start	44557961:44557961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315323
Start	44558987:44558987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1299C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315323
Start	44559233:44559233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1545G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315323
Start	44558993:44558993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315323
Start	44557892:44557892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FZD2

No Mutation Annotation!