Colon Cancer: Gene >> POLA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24809922:24809922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2971G>A
AA Mutation	p.Val991Ile(p.V991I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24741407:24741407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2231A>G
AA Mutation	p.His744Arg(p.H744R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24748889:24748889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2843C>T
AA Mutation	p.Ala948Val(p.A948V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24748903:24748903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2857G>T
AA Mutation	p.Ala953Ser(p.A953S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24741400:24741400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2224T>G
AA Mutation	p.Leu742Val(p.L742V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24888037:24888037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780353506
CDS Mutation	c.4061G>A
AA Mutation	p.Arg1354His(p.R1354H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379059
Start	24716453:24716453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200756660
CDS Mutation	c.599C>T
AA Mutation	p.Thr200Met(p.T200M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24735442:24735442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1859G>A
AA Mutation	p.Gly620Asp(p.G620D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24737684:24737684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1965A>C
AA Mutation	p.Lys655Asn(p.K655N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24739405:24739405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2053A>T
AA Mutation	p.Thr685Ser(p.T685S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24714637:24714637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412T>C
AA Mutation	p.Phe138Leu(p.F138L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24843604:24843604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3956C>A
AA Mutation	p.Pro1319His(p.P1319H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24739446:24739446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2094G>T
AA Mutation	p.Lys698Asn(p.K698N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379059
Start	24715167:24715167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379059
Start	24727876:24727876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189663317
CDS Mutation	c.1608G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379059
Start	24703301:24703301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379059
Start	24745476:24745477(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2607_2608insATTAAAAG
AA Mutation	p.Gln870IlefsTer40(p.Q870Ifs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379059
Start	24745478:24745479(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2609_2610insCT
AA Mutation	p.Gln870HisfsTer38(p.Q870Hfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> POLA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24748323:24748323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2686G>C
AA Mutation	p.Glu896Gln(p.E896Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24717360:24717360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759C>G
AA Mutation	p.Asp253Glu(p.D253E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24888043:24888043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4067G>A
AA Mutation	p.Arg1356Gln(p.R1356Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24812710:24812710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3125G>A
AA Mutation	p.Gly1042Glu(p.G1042E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24699474:24699474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75A>C
AA Mutation	p.Lys25Asn(p.K25N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379059
Start	24841800:24841800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3867G>T
AA Mutation	p.Glu1289Asp(p.E1289D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379059
Start	24748452:24748453(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2817dupT
AA Mutation	p.Leu940SerfsTer4(p.L940Sfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript