Colon Cancer: Gene >> UHRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4960762:4960762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2341G>A
AA Mutation	p.Val781Ile(p.V781I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4944154:4944154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096G>T
AA Mutation	p.Asp366Tyr(p.D366Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4932791:4932791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620G>C
AA Mutation	p.Arg207Pro(p.R207P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4932791:4932791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756642363
CDS Mutation	c.620G>A
AA Mutation	p.Arg207His(p.R207H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4929457:4929457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371706472
CDS Mutation	c.389C>T
AA Mutation	p.Thr130Met(p.T130M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4950968:4950968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1790G>A
AA Mutation	p.Arg597Gln(p.R597Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4960699:4960699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2278C>A
AA Mutation	p.Pro760Thr(p.P760T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612630
Start	4941902:4941902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612630
Start	4954762:4954762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748982378
CDS Mutation	c.2070C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612630
Start	4930721:4930721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612630
Start	4950614:4950614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775286606
CDS Mutation	c.1521G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612630
Start	4956741:4956741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769444008
CDS Mutation	c.2163G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612630
Start	4929407:4929407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UHRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4929342:4929342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.274G>A
AA Mutation	p.Asp92Asn(p.D92N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000612630
Start	4941828:4941828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Trp(p.R324W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript