Colon Cancer: Gene >> MCM7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100092973:100092973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2119T>C
AA Mutation	p.Trp707Arg(p.W707R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100100034:100100034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91T>C
AA Mutation	p.Phe31Leu(p.F31L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100092990:100092990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2102A>G
AA Mutation	p.Tyr701Cys(p.Y701C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000303887
Start	100095775:100095775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775586840
CDS Mutation	c.1594C>T
AA Mutation	p.Arg532Trp(p.R532W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100098625:100098625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752275987
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Trp(p.R225W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100095793:100095793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765971073
CDS Mutation	c.1576G>A
AA Mutation	p.Asp526Asn(p.D526N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100098194:100098194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778913504
CDS Mutation	c.817G>A
AA Mutation	p.Val273Ile(p.V273I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100097881:100097881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938A>C
AA Mutation	p.Glu313Ala(p.E313A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100099723:100099723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142C>A
AA Mutation	p.Leu48Met(p.L48M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000303887
Start	100094340:100094340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755556849
CDS Mutation	c.1681C>T
AA Mutation	p.Arg561Cys(p.R561C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100094250:100094250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771G>A
AA Mutation	p.Glu591Lys(p.E591K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100097914:100097914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767546167
CDS Mutation	c.905G>A
AA Mutation	p.Arg302Gln(p.R302Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303887
Start	100095944:100095944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1425C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303887
Start	100097732:100097732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146340949
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303887
Start	100096151:100096151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775965154
CDS Mutation	c.1218C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303887
Start	100094266:100094266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762734756
CDS Mutation	c.1755C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303887
Start	100099313:100099313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.367delC
AA Mutation	p.Gln123ArgfsTer26(p.Q123Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303887
Start	100095422:100095422(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1644delC
AA Mutation	p.Ser549ProfsTer8(p.S549Pfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MCM7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100099749:100099749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116G>A
AA Mutation	p.Arg39Gln(p.R39Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303887
Start	100093061:100093061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2031C>A
AA Mutation	p.Phe677Leu(p.F677L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303887
Start	100097732:100097732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146340949
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript