Colon Cancer: Gene >> USP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84759941:84759941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445G>T
AA Mutation	p.Arg482Leu(p.R482L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84778919:84778919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538632016
CDS Mutation	c.2234C>T
AA Mutation	p.Ala745Val(p.A745V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84758767:84758767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415His(p.R415H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84778955:84778955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2270T>A
AA Mutation	p.Ile757Asn(p.I757N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84744947:84744947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466C>T
AA Mutation	p.Pro156Ser(p.P156S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84772662:84772662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2120C>A
AA Mutation	p.Pro707His(p.P707H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84775205:84775205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779592460
CDS Mutation	c.2189G>A
AA Mutation	p.Arg730Gln(p.R730Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84768282:84768282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1922G>A
AA Mutation	p.Arg641His(p.R641H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84764202:84764202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780433322
CDS Mutation	c.1771G>A
AA Mutation	p.Val591Ile(p.V591I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84768230:84768230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1870A>G
AA Mutation	p.Thr624Ala(p.T624A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84768288:84768288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1928T>C
AA Mutation	p.Val643Ala(p.V643A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219473
Start	84759446:84759446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1368T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219473
Start	84779053:84779053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376147375
CDS Mutation	c.2368C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219473
Start	84760215:84760215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1494C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219473
Start	84760188:84760188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771982379
CDS Mutation	c.1467C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000219473
Start	84768320:84768320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960G>T
AA Mutation	p.Glu654Ter(p.E654*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> USP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84779044:84779044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2359G>A
AA Mutation	p.Ala787Thr(p.A787T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84733450:84733450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37T>G
AA Mutation	p.Phe13Val(p.F13V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219473
Start	84775190:84775190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2174A>C
AA Mutation	p.Asn725Thr(p.N725T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219473
Start	84744664:84744664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537583328
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000219473
Start	84772604:84772604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2062C>T
AA Mutation	p.Arg688Ter(p.R688*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript