Colon Cancer: Gene >> UCP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262999
Start	140562218:140562218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772583342
CDS Mutation	c.784G>A
AA Mutation	p.Glu262Lys(p.E262K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262999
Start	140568623:140568623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107C>T
AA Mutation	p.Thr36Met(p.T36M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262999
Start	140567794:140567794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310A>G
AA Mutation	p.Thr104Ala(p.T104A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262999
Start	140562259:140562259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743A>G
AA Mutation	p.Tyr248Cys(p.Y248C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262999
Start	140563327:140563327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517C>A
AA Mutation	p.Leu173Ile(p.L173I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262999
Start	140567830:140567830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274A>G
AA Mutation	p.Arg92Gly(p.R92G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262999
Start	140567892:140567892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776166009
CDS Mutation	c.212G>A
AA Mutation	p.Arg71Gln(p.R71Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262999
Start	140559967:140559967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853A>T
AA Mutation	p.Met285Leu(p.M285L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262999
Start	140568673:140568673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262999
Start	140568622:140568622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262999
Start	140563364:140563364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769473091
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262999
Start	140563454:140563454(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.390delT
AA Mutation	p.Ile130MetfsTer8(p.I130Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000262999
Start	140559969:140559970(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.850_851insGTGAATAAG
AA Mutation	p.Ile284delinsSerGluTerVal(p.I284delinsSE*V)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UCP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262999
Start	140562369:140562369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript