Colon Cancer: Gene >> FZD8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35639409:35639409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2021C>T
AA Mutation	p.Thr674Met(p.T674M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35640598:35640598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>A
AA Mutation	p.Val278Ile(p.V278I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35641029:35641029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401G>A
AA Mutation	p.Arg134His(p.R134H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35641155:35641155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275A>G
AA Mutation	p.Tyr92Cys(p.Y92C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35640127:35640127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303G>A
AA Mutation	p.Ala435Thr(p.A435T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35639738:35639738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640248:35640248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640185:35640185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1245G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640032:35640032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1398G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35641115:35641115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640128:35640128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35641352:35641352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35639876:35639876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640176:35640176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FZD8

No Mutation Annotation!