Colon Cancer: Gene >> USP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49278890:49278890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2657C>T
AA Mutation	p.Ala886Val(p.A886V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49300564:49300564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1415A>C
AA Mutation	p.Asp472Ala(p.D472A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49310678:49310678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896C>A
AA Mutation	p.Pro299His(p.P299H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49300673:49300673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306T>C
AA Mutation	p.Trp436Arg(p.W436R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49305741:49305741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546430537
CDS Mutation	c.1102G>A
AA Mutation	p.Ala368Thr(p.A368T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49294540:49294540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750T>G
AA Mutation	p.Phe584Val(p.F584V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49310664:49310664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910C>T
AA Mutation	p.Leu304Phe(p.L304F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49297955:49297955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760275117
CDS Mutation	c.1606G>A
AA Mutation	p.Ala536Thr(p.A536T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49286136:49286136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2162A>T
AA Mutation	p.Asn721Ile(p.N721I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265560
Start	49286201:49286201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2097C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265560
Start	49278844:49278844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745532309
CDS Mutation	c.2703C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265560
Start	49311642:49311642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143637177
CDS Mutation	c.708G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265560
Start	49298606:49298606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1542T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000265560
Start	49327778:49327778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268G>T
AA Mutation	p.Glu90Ter(p.E90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265560
Start	49311513:49311513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.836+1delG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> USP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265560
Start	49294571:49294571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1719T>A
AA Mutation	p.Asp573Glu(p.D573E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265560
Start	49278359:49278359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2826G>A
Mutation Classification	Silent
Feature Type	Transcript