Colon Cancer: Gene >> PLAA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397292
Start	26917138:26917138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140970730
CDS Mutation	c.1445C>T
AA Mutation	p.Ser482Leu(p.S482L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397292
Start	26907899:26907899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1757G>C
AA Mutation	p.Ser586Thr(p.S586T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397292
Start	26920309:26920309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558228832
CDS Mutation	c.1115G>A
AA Mutation	p.Gly372Glu(p.G372E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397292
Start	26926412:26926412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397292
Start	26928311:26928311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397292
Start	26935197:26935197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397292
Start	26913898:26913898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370264645
CDS Mutation	c.1536C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397292
Start	26910391:26910394(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1601_1604delATTT
AA Mutation	p.Tyr534SerfsTer18(p.Y534Sfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000397292
Start	26906077:26906077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1823-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000397292
Start	26928098:26928098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLAA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397292
Start	26906047:26906047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1852C>T
AA Mutation	p.Arg618Trp(p.R618W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397292
Start	26935021:26935021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335A>C
AA Mutation	p.Lys112Thr(p.K112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397292
Start	26907957:26907957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1699A>C
AA Mutation	p.Lys567Gln(p.K567Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397292
Start	26910423:26910423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1572A>C
Mutation Classification	Silent
Feature Type	Transcript