Colon Cancer: Gene >> PLXDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315392
Start	39107429:39107429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146173470
CDS Mutation	c.689G>A
AA Mutation	p.Arg230His(p.R230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315392
Start	39087695:39087695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.819G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315392
Start	39083515:39083515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375508586
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000315392
Start	39072448:39072448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1222+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLXDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315392
Start	39139791:39139791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.118A>G
AA Mutation	p.Thr40Ala(p.T40A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315392
Start	39109259:39109259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143773186
CDS Mutation	c.388C>T
AA Mutation	p.Arg130Trp(p.R130W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315392
Start	39069926:39069926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764949516
CDS Mutation	c.1313C>T
AA Mutation	p.Ala438Val(p.A438V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript