Colon Cancer: Gene >> PDLIM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284770
Start	185508501:185508501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460A>G
AA Mutation	p.Ser154Gly(p.S154G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284770
Start	185506638:185506638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747243505
CDS Mutation	c.677C>T
AA Mutation	p.Ser226Leu(p.S226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284770
Start	185514290:185514290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>A
AA Mutation	p.Phe126Leu(p.F126L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284770
Start	185506600:185506600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142143310
CDS Mutation	c.715G>A
AA Mutation	p.Asp239Asn(p.D239N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284770
Start	185525028:185525028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284770
Start	185508499:185508499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284770
Start	185506565:185506565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146946948
CDS Mutation	c.750G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PDLIM3

Mutation ID	1
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000284770
Start	185523361:185523361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript