Colon Cancer: Gene >> WNT8A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398754
Start	138088959:138088959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>A
AA Mutation	p.Asp134Asn(p.D134N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398754
Start	138090697:138090697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680C>T
AA Mutation	p.Ala227Val(p.A227V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398754
Start	138090757:138090757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740C>T
AA Mutation	p.Ala247Val(p.A247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398754
Start	138089018:138089018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774394129
CDS Mutation	c.459G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398754
Start	138088982:138088982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WNT8A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398754
Start	138090730:138090730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713C>T
AA Mutation	p.Ala238Val(p.A238V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript