Colon Cancer: Gene >> UHRF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6477754:6477754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773132991
CDS Mutation	c.1106A>T
AA Mutation	p.Tyr369Phe(p.Y369F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6434071:6434071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542A>C
AA Mutation	p.Lys181Thr(p.K181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6498129:6498129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879C>T
AA Mutation	p.Arg627Trp(p.R627W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6460623:6460623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>A
AA Mutation	p.Arg232Gln(p.R232Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6477715:6477715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067C>A
AA Mutation	p.Pro356His(p.P356H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6413561:6413561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71C>T
AA Mutation	p.Thr24Met(p.T24M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6493878:6493878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550G>T
AA Mutation	p.Gly517Val(p.G517V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6497290:6497290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697G>A
AA Mutation	p.Arg566His(p.R566H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6413582:6413582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92G>A
AA Mutation	p.Arg31Gln(p.R31Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6486894:6486894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1466T>G
AA Mutation	p.Leu489Arg(p.L489R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6493884:6493884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1556A>C
AA Mutation	p.Lys519Thr(p.K519T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276893
Start	6504599:6504599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276893
Start	6475442:6475442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276893
Start	6504628:6504628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760957476
CDS Mutation	c.2199C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276893
Start	6481759:6481759(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1280delG
AA Mutation	p.Gly427AlafsTer39(p.G427Afs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UHRF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276893
Start	6497341:6497341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1748G>T
AA Mutation	p.Arg583Ile(p.R583I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript