Colon Cancer: Gene >> POLD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406581
Start	44118001:44118001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284G>C
AA Mutation	p.Gly95Ala(p.G95A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000406581
Start	44116245:44116245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889G>T
AA Mutation	p.Gly297Cys(p.G297C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000406581
Start	44117155:44117155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768064825
CDS Mutation	c.559G>A
AA Mutation	p.Ala187Thr(p.A187T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000406581
Start	44114817:44114817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752936314
CDS Mutation	c.1378G>A
AA Mutation	p.Asp460Asn(p.D460N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406581
Start	44116913:44116913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144701499
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406581
Start	44116243:44116243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368138685
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406581
Start	44116868:44116868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762376881
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406581
Start	44115878:44115878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406581
Start	44121860:44121863(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.191_194delTCCT
AA Mutation	p.Phe64TrpfsTer15(p.F64Wfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000406581
Start	44115895:44115895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> POLD2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406581
Start	44115881:44115881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1032A>G
Mutation Classification	Silent
Feature Type	Transcript