Colon Cancer: Gene >> MCM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47976768:47976768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2582G>A
AA Mutation	p.Arg861His(p.R861H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47973008:47973008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777231755
CDS Mutation	c.2080G>A
AA Mutation	p.Ala694Thr(p.A694T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47962188:47962188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>T
AA Mutation	p.Gly124Val(p.G124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47966381:47966381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768182076
CDS Mutation	c.1027C>T
AA Mutation	p.Arg343Cys(p.R343C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47972915:47972915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1987G>T
AA Mutation	p.Ala663Ser(p.A663S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47971366:47971366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1826C>T
AA Mutation	p.Ala609Val(p.A609V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47961641:47961641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.196G>C
AA Mutation	p.Asp66His(p.D66H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47969976:47969976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353A>C
AA Mutation	p.Glu451Asp(p.E451D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262105
Start	47966338:47966338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200670710
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262105
Start	47971419:47971419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1885delA
AA Mutation	p.Thr629GlnfsTer18(p.T629Qfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262105
Start	47961200:47961200(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.60delC
AA Mutation	p.Ala21ProfsTer70(p.A21Pfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262105
Start	47961640:47961640(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.196delG
AA Mutation	p.Asp66ThrfsTer25(p.D66Tfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000262105
Start	47969821:47969821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
AA Mutation	p.Arg400Ter(p.R400*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000262105
Start	47969806:47969806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183C>T
AA Mutation	p.Arg395Ter(p.R395*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000262105
Start	47974804:47974804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2207C>A
AA Mutation	p.Ser736Ter(p.S736*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262105
Start	47962944:47962944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262105
Start	47962763:47962763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MCM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47969954:47969954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1331A>C
AA Mutation	p.Lys444Thr(p.K444T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47962065:47962065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248A>C
AA Mutation	p.Asp83Ala(p.D83A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262105
Start	47975777:47975777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2428T>G
AA Mutation	p.Leu810Val(p.L810V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262105
Start	47970804:47970804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148525401
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262105
Start	47974850:47974850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780201599
CDS Mutation	c.2253C>T
Mutation Classification	Silent
Feature Type	Transcript