Colon Cancer: Gene >> EXO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241867016:241867016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228C>A
AA Mutation	p.Leu410Ile(p.L410I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241852304:241852304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174T>A
AA Mutation	p.Phe58Leu(p.F58L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241878823:241878823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589T>C
AA Mutation	p.Val530Ala(p.V530A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241879096:241879096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367935074
CDS Mutation	c.1862C>T
AA Mutation	p.Thr621Met(p.T621M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241853444:241853444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368T>C
AA Mutation	p.Ile123Thr(p.I123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241889505:241889505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2446C>A
AA Mutation	p.Pro816Thr(p.P816T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241866852:241866852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1064G>C
AA Mutation	p.Ser355Thr(p.S355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241878925:241878925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751493652
CDS Mutation	c.1691C>T
AA Mutation	p.Pro564Leu(p.P564L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241872087:241872087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323G>T
AA Mutation	p.Lys441Asn(p.K441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241850486:241850486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61A>G
AA Mutation	p.Lys21Glu(p.K21E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241885454:241885454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2352G>T
AA Mutation	p.Lys784Asn(p.K784N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241885457:241885457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61751859
CDS Mutation	c.2355G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241866847:241866847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241878971:241878971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241879295:241879295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2061A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241879187:241879187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1953G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348581
Start	241853407:241853407(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.333delA
AA Mutation	p.Val112SerfsTer22(p.V112Sfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EXO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241853363:241853363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764989865
CDS Mutation	c.287G>A
AA Mutation	p.Arg96Gln(p.R96Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000348581
Start	241878870:241878870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1636G>T
AA Mutation	p.Glu546Ter(p.E546*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000348581
Start	241872025:241872052(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1268-6_1289delATTTAGCAGAGCTGTCAGAAGATGACCT
Mutation Classification	Splice_Site
Feature Type	Transcript