Colon Cancer: Gene >> WNT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290167
Start	22129640:22129640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760357534
CDS Mutation	c.289G>A
AA Mutation	p.Val97Ile(p.V97I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290167
Start	22129682:22129682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121908652
CDS Mutation	c.247C>T
AA Mutation	p.Arg83Trp(p.R83W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290167
Start	22129804:22129804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125C>T
AA Mutation	p.Thr42Met(p.T42M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290167
Start	22121263:22121263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>A
AA Mutation	p.Ala179Asp(p.A179D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290167
Start	22120314:22120314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290167
Start	22121482:22121482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753168607
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000290167
Start	22129853:22129853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WNT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290167
Start	22129844:22129844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript