Colon Cancer: Gene >> UBTD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570174:97570174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570302:97570302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463C>A
AA Mutation	p.Leu155Met(p.L155M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570348:97570348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509C>T
AA Mutation	p.Thr170Ile(p.T170I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370664
Start	97570451:97570451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370664
Start	97568026:97568026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763391490
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370664
Start	97570310:97570310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758894209
CDS Mutation	c.471G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370664
Start	97570352:97570352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UBTD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570207:97570207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146047099
CDS Mutation	c.368C>T
AA Mutation	p.Pro123Leu(p.P123L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript