Colon Cancer: Gene >> WNT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233948
Start	218871701:218871701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518G>A
AA Mutation	p.Gly173Asp(p.G173D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233948
Start	218871671:218871671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375682009
CDS Mutation	c.488G>A
AA Mutation	p.Gly163Asp(p.G163D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233948
Start	218873448:218873448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701G>A
AA Mutation	p.Arg234His(p.R234H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233948
Start	218871666:218871666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751090791
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WNT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233948
Start	218871082:218871082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766635655
CDS Mutation	c.136C>T
AA Mutation	p.Arg46Trp(p.R46W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript