Colon Cancer: Gene >> OGT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71557653:71557653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1583G>A
AA Mutation	p.Gly528Asp(p.G528D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71573633:71573633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2980C>T
AA Mutation	p.Arg994Cys(p.R994C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71555284:71555284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823A>G
AA Mutation	p.Ile275Val(p.I275V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71544591:71544591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487C>A
AA Mutation	p.Leu163Met(p.L163M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71567557:71567557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2647G>C
AA Mutation	p.Glu883Gln(p.E883Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71568106:71568106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2956G>C
AA Mutation	p.Asp986His(p.D986H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71563351:71563351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2288A>G
AA Mutation	p.Asp763Gly(p.D763G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373719
Start	71562948:71562948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770630335
CDS Mutation	c.2079C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373719
Start	71562882:71562882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148161543
CDS Mutation	c.2013G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000373719
Start	71567554:71567554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2644G>T
AA Mutation	p.Gly882Ter(p.G882*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373719
Start	71538046:71538047(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.436_437insCTGCC
AA Mutation	p.Tyr146SerfsTer38(p.Y146Sfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000373719
Start	71555953:71555953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> OGT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71562952:71562952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083A>G
AA Mutation	p.Lys695Glu(p.K695E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71556027:71556027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998T>C
AA Mutation	p.Leu333Pro(p.L333P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71561897:71561897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1974T>G
AA Mutation	p.Ile658Met(p.I658M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373719
Start	71568042:71568042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2892T>G
Mutation Classification	Silent
Feature Type	Transcript