Colon Cancer: Gene >> ARMC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23037315:23037315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2455G>A
AA Mutation	p.Glu819Lys(p.E819K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23030635:23030635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2085G>T
AA Mutation	p.Glu695Asp(p.E695D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23030599:23030599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2049A>C
AA Mutation	p.Lys683Asn(p.K683N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23001931:23001931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438G>T
AA Mutation	p.Gly480Cys(p.G480C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	22998296:22998296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324C>T
AA Mutation	p.His442Tyr(p.H442Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	22981400:22981400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.977G>C
AA Mutation	p.Gly326Ala(p.G326A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	22998356:22998356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769301977
CDS Mutation	c.1384G>A
AA Mutation	p.Ala462Thr(p.A462T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23001992:23001992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1499C>T
AA Mutation	p.Ala500Val(p.A500V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23037325:23037325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2465G>C
AA Mutation	p.Arg822Thr(p.R822T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	22968418:22968418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845T>C
AA Mutation	p.Phe282Ser(p.F282S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23006894:23006894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1742G>A
AA Mutation	p.Gly581Asp(p.G581D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23008332:23008332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1886C>A
AA Mutation	p.Ser629Tyr(p.S629Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23008852:23008852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1966C>A
AA Mutation	p.Pro656Thr(p.P656T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23033007:23033007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372574174
CDS Mutation	c.2393G>A
AA Mutation	p.Arg798Gln(p.R798Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	22998267:22998267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140763346
CDS Mutation	c.1295G>A
AA Mutation	p.Arg432His(p.R432H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23032934:23032934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2320A>C
AA Mutation	p.Ser774Arg(p.S774R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23001986:23001986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1493A>C
AA Mutation	p.Lys498Thr(p.K498T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	22962061:22962061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715A>C
AA Mutation	p.Lys239Gln(p.K239Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298032
Start	22998268:22998268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298032
Start	23037320:23037320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762403977
CDS Mutation	c.2460C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298032
Start	23030677:23030677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2127A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298032
Start	23008911:23008911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2025C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298032
Start	22981394:22981394(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.974delT
AA Mutation	p.Leu325TrpfsTer37(p.L325Wfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298032
Start	23030608:23030608(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2064delA
AA Mutation	p.Glu689LysfsTer5(p.E689Kfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000298032
Start	22981616:22981616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091T>A
AA Mutation	p.Leu364Ter(p.L364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298032
Start	22932035:22932036(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.41dupA
AA Mutation	p.Asp15GlyfsTer4(p.D15Gfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298032
Start	23030607:23030608(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2064dupA
AA Mutation	p.Glu689ArgfsTer20(p.E689Rfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARMC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	22981661:22981661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1136C>T
AA Mutation	p.Ala379Val(p.A379V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	22959079:22959079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302A>C
AA Mutation	p.Lys101Thr(p.K101T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298032
Start	23037309:23037309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2449C>T
AA Mutation	p.Arg817Cys(p.R817C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000298032
Start	22961896:22961896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201134940
CDS Mutation	c.550C>T
AA Mutation	p.Arg184Ter(p.R184*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000298032
Start	23003265:23003265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1582G>T
AA Mutation	p.Glu528Ter(p.E528*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript