Colon Cancer: Gene >> USP11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47240632:47240632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Ala286Thr(p.A286T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47239413:47239413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478G>A
AA Mutation	p.Ala160Thr(p.A160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47242704:47242704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1696C>T
AA Mutation	p.Arg566Cys(p.R566C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47240358:47240358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718A>G
AA Mutation	p.Thr240Ala(p.T240A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47247670:47247670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2725G>A
AA Mutation	p.Val909Ile(p.V909I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47247799:47247799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2761G>A
AA Mutation	p.Ala921Thr(p.A921T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47242512:47242512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1607C>T
AA Mutation	p.Ser536Leu(p.S536L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218348
Start	47241621:47241621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776567388
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218348
Start	47244534:47244534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143527670
CDS Mutation	c.1956C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218348
Start	47243432:47243432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1749C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218348
Start	47233076:47233076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218348
Start	47247831:47247831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768509072
CDS Mutation	c.2793C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218348
Start	47241693:47241693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201389587
CDS Mutation	c.1302G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218348
Start	47241345:47241345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218348
Start	47243528:47243528(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1849delC
AA Mutation	p.Leu617SerfsTer19(p.L617Sfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218348
Start	47244537:47244538(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1963dupG
AA Mutation	p.Asp655GlyfsTer2(p.D655Gfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> USP11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47242287:47242287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1514C>T
AA Mutation	p.Pro505Leu(p.P505L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218348
Start	47247816:47247816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2778C>A
AA Mutation	p.Phe926Leu(p.F926L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218348
Start	47243528:47243528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1845C>T
Mutation Classification	Silent
Feature Type	Transcript