Colon Cancer: Gene >> MCM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5954616:5954616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189649618
CDS Mutation	c.262G>A
AA Mutation	p.Asp88Asn(p.D88N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5973134:5973134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369169161
CDS Mutation	c.1333C>T
AA Mutation	p.Arg445Trp(p.R445W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5984944:5984944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897T>G
AA Mutation	p.Ser633Ala(p.S633A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5952487:5952487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212G>A
AA Mutation	p.Arg71Gln(p.R71Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5977903:5977903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376216985
CDS Mutation	c.1423G>A
AA Mutation	p.Val475Met(p.V475M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5963290:5963290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806G>A
AA Mutation	p.Cys269Tyr(p.C269Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378896
Start	5954615:5954615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752298258
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378896
Start	5983161:5983161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1729T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378896
Start	5967445:5967445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000378896
Start	5958728:5958728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MCM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5958658:5958658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721C>A
AA Mutation	p.Leu241Ile(p.L241I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5984840:5984840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1793A>T
AA Mutation	p.Asn598Ile(p.N598I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5984960:5984960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1913T>C
AA Mutation	p.Leu638Pro(p.L638P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5963321:5963321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>A
AA Mutation	p.Ser279Arg(p.S279R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5986121:5986121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772901194
CDS Mutation	c.2153G>A
AA Mutation	p.Arg718His(p.R718H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378896
Start	5952113:5952114(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.98_99insC
AA Mutation	p.Glu33AspfsTer7(p.E33Dfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript