Colon Cancer: Gene >> MCM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229854
Start	52264596:52264596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2419C>A
AA Mutation	p.Leu807Ile(p.L807I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229854
Start	52273745:52273745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546G>A
AA Mutation	p.Asp516Asn(p.D516N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229854
Start	52264726:52264726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2289C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MCM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229854
Start	52283321:52283321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750663816
CDS Mutation	c.164G>A
AA Mutation	p.Arg55His(p.R55H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229854
Start	52282164:52282164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371347878
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Cys(p.R138C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229854
Start	52282148:52282148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765811660
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000229854
Start	52276414:52276414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1228G>T
AA Mutation	p.Glu410Ter(p.E410*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript