Colon Cancer: Gene >> USP5

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000229268
Start	6857631:6857631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200664735
CDS Mutation	c.772G>A
AA Mutation	p.Val258Met(p.V258M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6860376:6860376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1229A>C
AA Mutation	p.Asp410Ala(p.D410A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6865184:6865184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2419A>G
AA Mutation	p.Ile807Val(p.I807V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6860379:6860379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232G>A
AA Mutation	p.Gly411Asp(p.G411D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6862499:6862499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1703A>G
AA Mutation	p.Tyr568Cys(p.Y568C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6856438:6856438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572G>A
AA Mutation	p.Arg191Gln(p.R191Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6855807:6855807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290C>T
AA Mutation	p.Thr97Met(p.T97M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000229268
Start	6856148:6856148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369790819
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Trp(p.R146W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6856106:6856106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394G>C
AA Mutation	p.Ala132Pro(p.A132P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6861022:6861022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1414C>A
AA Mutation	p.Leu472Met(p.L472M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6864100:6864100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2149A>C
AA Mutation	p.Ser717Arg(p.S717R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6855804:6855804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287C>T
AA Mutation	p.Pro96Leu(p.P96L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229268
Start	6863214:6863214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782615732
CDS Mutation	c.1791C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229268
Start	6855415:6855415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229268
Start	6856809:6856809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229268
Start	6858531:6858531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229268
Start	6855484:6855484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764601063
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229268
Start	6864114:6864114(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2168delC
AA Mutation	p.Pro723LeufsTer6(p.P723Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000229268
Start	6855491:6855491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Ter(p.R68*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229268
Start	6859493:6859494(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1082_1083insA
AA Mutation	p.Phe362LeufsTer66(p.F362Lfs*66)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> USP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6860997:6860997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1389C>A
AA Mutation	p.Phe463Leu(p.F463L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6863332:6863332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909G>A
AA Mutation	p.Glu637Lys(p.E637K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6855807:6855807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290C>G
AA Mutation	p.Thr97Arg(p.T97R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229268
Start	6864794:6864794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2317G>A
AA Mutation	p.Asp773Asn(p.D773N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript