Colon Cancer: Gene >> USP36

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78798481:78798481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753159695
CDS Mutation	c.3311G>A
AA Mutation	p.Arg1104Gln(p.R1104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78818749:78818749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199873425
CDS Mutation	c.941G>A
AA Mutation	p.Arg314His(p.R314H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78803620:78803620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763096707
CDS Mutation	c.2575G>A
AA Mutation	p.Ala859Thr(p.A859T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78828924:78828924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Pro187Ser(p.P187S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78828933:78828933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139783752
CDS Mutation	c.550G>A
AA Mutation	p.Ala184Thr(p.A184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78799699:78799699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3092A>C
AA Mutation	p.Lys1031Thr(p.K1031T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78803466:78803466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2729C>A
AA Mutation	p.Ala910Glu(p.A910E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78821023:78821023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777212345
CDS Mutation	c.796G>A
AA Mutation	p.Asp266Asn(p.D266N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78828948:78828948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201774114
CDS Mutation	c.535G>A
AA Mutation	p.Ala179Thr(p.A179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000542802
Start	78827309:78827309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.625G>A
AA Mutation	p.Ala209Thr(p.A209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542802
Start	78836148:78836148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542802
Start	78799677:78799677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138761721
CDS Mutation	c.3114C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542802
Start	78814496:78814496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542802
Start	78813820:78813820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558007542
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000542802
Start	78806980:78806980(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2064delA
AA Mutation	p.Lys688AsnfsTer35(p.K688Nfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_lost
Transcription ID	ENST00000542802
Start	78798422:78798422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3370T>C
AA Mutation	p.Ter1124ArgextTer56(p.*1124Rext*56)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> USP36

No Mutation Annotation!