Colon Cancer: Gene >> PADI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17069190:17069190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572228579
CDS Mutation	c.1852G>A
AA Mutation	p.Val618Met(p.V618M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17074927:17074927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1478G>A
AA Mutation	p.Ser493Asn(p.S493N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17082613:17082613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>T
AA Mutation	p.Gly364Cys(p.G364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17069187:17069187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149369913
CDS Mutation	c.1855C>T
AA Mutation	p.Arg619Cys(p.R619C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17105045:17105045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109G>A
AA Mutation	p.Ala37Thr(p.A37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17075687:17075687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371989695
CDS Mutation	c.1447G>A
AA Mutation	p.Gly483Ser(p.G483S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17104993:17104993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367699636
CDS Mutation	c.161G>A
AA Mutation	p.Arg54His(p.R54H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375486
Start	17084693:17084693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375486
Start	17084670:17084670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187500985
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PADI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17086601:17086601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192937557
CDS Mutation	c.754G>A
AA Mutation	p.Val252Met(p.V252M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375486
Start	17070212:17070212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1640G>A
AA Mutation	p.Cys547Tyr(p.C547Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375486
Start	17086689:17086689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141669259
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript