Colon Cancer: Gene >> MCM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265056
Start	127604637:127604637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266C>T
AA Mutation	p.Ala89Val(p.A89V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265056
Start	127616933:127616933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1588T>C
AA Mutation	p.Ser530Pro(p.S530P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265056
Start	127621154:127621154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2530G>A
AA Mutation	p.Val844Met(p.V844M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265056
Start	127599423:127599423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112C>A
AA Mutation	p.Leu38Ile(p.L38I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265056
Start	127618062:127618062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1994A>T
AA Mutation	p.Asp665Val(p.D665V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265056
Start	127619039:127619039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2026G>T
AA Mutation	p.Ala676Ser(p.A676S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265056
Start	127619191:127619191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776426152
CDS Mutation	c.2178C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265056
Start	127604969:127604969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265056
Start	127617392:127617392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141735401
CDS Mutation	c.1887C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265056
Start	127615933:127615933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757903789
CDS Mutation	c.1500C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265056
Start	127606718:127606718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376347464
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265056
Start	127599495:127599495(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.187delC
AA Mutation	p.Leu63TrpfsTer40(p.L63Wfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MCM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265056
Start	127615949:127615949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1516A>C
AA Mutation	p.Asn506His(p.N506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265056
Start	127606718:127606718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376347464
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265056
Start	127606796:127606796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080C>A
Mutation Classification	Silent
Feature Type	Transcript