Colon Cancer: Gene >> UTP14A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394422
Start	129911142:129911142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373A>T
AA Mutation	p.Ile125Phe(p.I125F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394422
Start	129925977:129925977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1808A>T
AA Mutation	p.Asp603Val(p.D603V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394422
Start	129924914:129924914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1468G>A
AA Mutation	p.Glu490Lys(p.E490K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394422
Start	129920484:129920484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780G>T
AA Mutation	p.Lys260Asn(p.K260N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394422
Start	129924811:129924811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365G>T
AA Mutation	p.Glu455Asp(p.E455D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394422
Start	129925160:129925160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1714G>A
AA Mutation	p.Val572Met(p.V572M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394422
Start	129926253:129926253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1957G>A
AA Mutation	p.Ala653Thr(p.A653T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394422
Start	129911834:129911834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394422
Start	129911078:129911078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.309G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000394422
Start	129919404:129919404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Ter(p.R223*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UTP14A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394422
Start	129920518:129920518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759581297
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Trp(p.R272W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394422
Start	129926065:129926065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1896C>T
Mutation Classification	Silent
Feature Type	Transcript