Colon Cancer: Gene >> USO1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000514213
Start	75757571:75757571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293T>A
AA Mutation	p.Val98Glu(p.V98E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000514213
Start	75724856:75724856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37G>A
AA Mutation	p.Ala13Thr(p.A13T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000514213
Start	75790702:75790702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773378481
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000514213
Start	75787068:75787068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370383563
CDS Mutation	c.862C>T
AA Mutation	p.Arg288Cys(p.R288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000514213
Start	75800430:75800430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201356959
CDS Mutation	c.1643C>T
AA Mutation	p.Ser548Leu(p.S548L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000514213
Start	75801193:75801193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752225678
CDS Mutation	c.1979G>A
AA Mutation	p.Arg660Gln(p.R660Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000514213
Start	75805237:75805237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2223A>T
AA Mutation	p.Glu741Asp(p.E741D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000514213
Start	75806560:75806560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2364A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000514213
Start	75800777:75800777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761243010
CDS Mutation	c.1842G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000514213
Start	75782746:75782747(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.750dupT
AA Mutation	p.Lys251Ter(p.K251*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000514213
Start	75812331:75812332(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2755_2756insC
AA Mutation	p.Lys919ThrfsTer8(p.K919Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000514213
Start	75812332:75812333(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2756_2757insGAGCTTT
AA Mutation	p.Ile920SerfsTer9(p.I920Sfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> USO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000514213
Start	75799706:75799706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1537C>A
AA Mutation	p.Leu513Ile(p.L513I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000514213
Start	75801192:75801192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1978C>T
AA Mutation	p.Arg660Ter(p.R660*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript