Colon Cancer: Gene >> PLVAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252590
Start	17376939:17376939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199706929
CDS Mutation	c.350G>A
AA Mutation	p.Arg117His(p.R117H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252590
Start	17365722:17365722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756937606
CDS Mutation	c.743G>A
AA Mutation	p.Arg248His(p.R248H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252590
Start	17365350:17365350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773739320
CDS Mutation	c.1115C>T
AA Mutation	p.Ala372Val(p.A372V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252590
Start	17376942:17376942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.347T>C
AA Mutation	p.Phe116Ser(p.F116S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252590
Start	17365493:17365493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.972G>T
AA Mutation	p.Lys324Asn(p.K324N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252590
Start	17377248:17377248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41C>A
AA Mutation	p.Ala14Glu(p.A14E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252590
Start	17377256:17377256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768034061
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252590
Start	17365679:17365679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252590
Start	17365502:17365502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150210307
CDS Mutation	c.963G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252590
Start	17377242:17377242(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.47delG
AA Mutation	p.Gly16AlafsTer39(p.G16Afs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLVAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252590
Start	17365549:17365549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Cys(p.R306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252590
Start	17366184:17366184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381G>A
Mutation Classification	Silent
Feature Type	Transcript