Colon Cancer: Gene >> MCM6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135870315:135870315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767037709
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Cys(p.R101C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135848157:135848157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949G>A
AA Mutation	p.Arg650Gln(p.R650Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135865043:135865043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1048C>A
AA Mutation	p.Leu350Ile(p.L350I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135856847:135856847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507G>A
AA Mutation	p.Ala503Thr(p.A503T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135862701:135862701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759630336
CDS Mutation	c.1126G>A
AA Mutation	p.Val376Ile(p.V376I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135844592:135844592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2302A>C
AA Mutation	p.Asn768His(p.N768H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135868669:135868669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557C>T
AA Mutation	p.Ala186Val(p.A186V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135844619:135844619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2275G>C
AA Mutation	p.Glu759Gln(p.E759Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264156
Start	135856863:135856863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1491G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264156
Start	135859424:135859424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760232150
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264156
Start	135844583:135844583(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2311delA
AA Mutation	p.Arg771GlufsTer3(p.R771Efs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264156
Start	135862732:135862732(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1095delA
AA Mutation	p.Lys365AsnfsTer6(p.K365Nfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000264156
Start	135866215:135866215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844C>T
AA Mutation	p.Arg282Ter(p.R282*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000264156
Start	135851464:135851464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1855C>T
AA Mutation	p.Arg619Ter(p.R619*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MCM6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135844645:135844645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754663697
CDS Mutation	c.2249A>G
AA Mutation	p.Asn750Ser(p.N750S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135856763:135856763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591G>A
AA Mutation	p.Asp531Asn(p.D531N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264156
Start	135862611:135862611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1216C>A
AA Mutation	p.Leu406Ile(p.L406I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264156
Start	135862702:135862702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767725842
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000264156
Start	135868856:135868856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Ter(p.R124*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript