Colon Cancer: Gene >> TRIM33

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358465
Start	114430799:114430799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154A>T
AA Mutation	p.Glu385Val(p.E385V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114402788:114402788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371685549
CDS Mutation	c.2864C>T
AA Mutation	p.Ala955Val(p.A955V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114463455:114463455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.747A>T
AA Mutation	p.Lys249Asn(p.K249N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114399596:114399596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2981A>G
AA Mutation	p.Tyr994Cys(p.Y994C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114405492:114405492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2686G>A
AA Mutation	p.Gly896Arg(p.G896R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114397731:114397731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3301G>A
AA Mutation	p.Val1101Ile(p.V1101I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114401460:114401460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2896T>C
AA Mutation	p.Cys966Arg(p.C966R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114430876:114430876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1077A>C
AA Mutation	p.Glu359Asp(p.E359D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114405471:114405471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748568840
CDS Mutation	c.2707G>A
AA Mutation	p.Glu903Lys(p.E903K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114421569:114421569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760094981
CDS Mutation	c.1928C>T
AA Mutation	p.Thr643Met(p.T643M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114463212:114463212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815G>A
AA Mutation	p.Arg272His(p.R272H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358465
Start	114433622:114433622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358465
Start	114433628:114433628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775641525
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358465
Start	114433679:114433679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358465
Start	114433673:114433673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358465
Start	114421568:114421568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768838621
CDS Mutation	c.1929G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000358465
Start	114405585:114405585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2593C>T
AA Mutation	p.Arg865Ter(p.R865*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358465
Start	114430809:114430810(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1143dupA
AA Mutation	p.Gln382ThrfsTer20(p.Q382Tfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358465
Start	114410281:114410282(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2096_2097insGGAGAATTCTG
AA Mutation	p.Leu700GlufsTer5(p.L700Efs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114401456:114401456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2900A>G
AA Mutation	p.Glu967Gly(p.E967G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114397795:114397795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3237G>T
AA Mutation	p.Glu1079Asp(p.E1079D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114425592:114425592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1552C>A
AA Mutation	p.His518Asn(p.H518N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358465
Start	114433698:114433698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959A>G
AA Mutation	p.Lys320Arg(p.K320R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript