Colon Cancer: Gene >> MME

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155142266:155142266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124T>G
AA Mutation	p.Phe375Cys(p.F375C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155180449:155180449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200966070
CDS Mutation	c.2243G>A
AA Mutation	p.Arg748Gln(p.R748Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155116910:155116910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578C>A
AA Mutation	p.Ser193Tyr(p.S193Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155140217:155140217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882T>A
AA Mutation	p.Asn294Lys(p.N294K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155116962:155116962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630G>T
AA Mutation	p.Lys210Asn(p.K210N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155115115:155115115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756048894
CDS Mutation	c.318C>A
AA Mutation	p.Asn106Lys(p.N106K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155140213:155140213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878G>A
AA Mutation	p.Arg293Gln(p.R293Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155142306:155142306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1164G>T
AA Mutation	p.Lys388Asn(p.K388N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000360490
Start	155168492:155168492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1781G>T
AA Mutation	p.Gly594Val(p.G594V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155142255:155142255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113G>A
AA Mutation	p.Met371Ile(p.M371I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155116921:155116921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746423553
CDS Mutation	c.589A>G
AA Mutation	p.Lys197Glu(p.K197E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155116532:155116532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412G>A
AA Mutation	p.Ala138Thr(p.A138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155138150:155138150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145687755
CDS Mutation	c.769C>T
AA Mutation	p.Arg257Cys(p.R257C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155084235:155084235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201850855
CDS Mutation	c.68G>A
AA Mutation	p.Arg23Gln(p.R23Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155116730:155116730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506T>A
AA Mutation	p.Val169Glu(p.V169E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155172602:155172602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2143G>A
AA Mutation	p.Gly715Ser(p.G715S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155115065:155115065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268G>T
AA Mutation	p.Gly90Cys(p.G90C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360490
Start	155115109:155115109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202011191
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360490
Start	155147167:155147167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777374821
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360490
Start	155084266:155084266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000360490
Start	155084328:155084328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000360490
Start	155116987:155116987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MME

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000360490
Start	155142328:155142328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1186A>G
AA Mutation	p.Lys396Glu(p.K396E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155140213:155140213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878G>A
AA Mutation	p.Arg293Gln(p.R293Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155142241:155142241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751199945
CDS Mutation	c.1099C>A
AA Mutation	p.Leu367Ile(p.L367I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360490
Start	155172152:155172152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2016A>C
AA Mutation	p.Glu672Asp(p.E672D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript