Colon Cancer: Gene >> MCM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216122
Start	35412659:35412659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1069C>T
AA Mutation	p.Leu357Phe(p.L357F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216122
Start	35406604:35406604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475T>G
AA Mutation	p.Ser159Ala(p.S159A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216122
Start	35406647:35406647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518G>A
AA Mutation	p.Arg173His(p.R173H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216122
Start	35416700:35416700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762680535
CDS Mutation	c.1476C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216122
Start	35403509:35403509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372421942
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216122
Start	35410810:35410810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.819G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216122
Start	35412658:35412658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1068G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216122
Start	35416398:35416398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137919698
CDS Mutation	c.1407C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216122
Start	35415876:35415876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370921899
CDS Mutation	c.1251G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000216122
Start	35416816:35416816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1590+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MCM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216122
Start	35416767:35416767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761749738
CDS Mutation	c.1543G>A
AA Mutation	p.Asp515Asn(p.D515N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216122
Start	35423264:35423264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756439766
CDS Mutation	c.2026G>A
AA Mutation	p.Glu676Lys(p.E676K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript