Colon Cancer: Gene >> FZD7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202036073:202036073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1426G>T
AA Mutation	p.Val476Leu(p.V476L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202035906:202035906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259C>T
AA Mutation	p.Ala420Val(p.A420V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202035915:202035915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268G>C
AA Mutation	p.Gly423Ala(p.G423A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202035584:202035584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937G>A
AA Mutation	p.Ala313Thr(p.A313T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202035144:202035144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185267840
CDS Mutation	c.497C>T
AA Mutation	p.Ser166Leu(p.S166L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202036319:202036319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1672C>T
AA Mutation	p.Arg558Cys(p.R558C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202036199:202036199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1552G>T
AA Mutation	p.Gly518Cys(p.G518C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202034963:202034963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316T>C
AA Mutation	p.Tyr106His(p.Y106H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202036050:202036050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403T>C
AA Mutation	p.Met468Thr(p.M468T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000286201
Start	202036100:202036100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1453G>A
AA Mutation	p.Val485Ile(p.V485I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202035421:202035421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202035358:202035358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202036120:202036120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1473C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202036030:202036030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202034731:202034731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202035526:202035526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202035802:202035802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202035448:202035448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286201
Start	202035232:202035232(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.589delG
AA Mutation	p.Ala197ProfsTer46(p.A197Pfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FZD7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286201
Start	202036297:202036297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1650G>A
Mutation Classification	Silent
Feature Type	Transcript