Colon Cancer: Gene >> GCNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10529054:10529054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143C>T
AA Mutation	p.Ala48Val(p.A48V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10529368:10529368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368989684
CDS Mutation	c.457G>A
AA Mutation	p.Ala153Thr(p.A153T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10626558:10626558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1160G>T
AA Mutation	p.Arg387Ile(p.R387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10529100:10529100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189T>G
AA Mutation	p.Asn63Lys(p.N63K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10529605:10529605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773968312
CDS Mutation	c.694G>A
AA Mutation	p.Val232Ile(p.V232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10529473:10529473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562A>G
AA Mutation	p.Ile188Val(p.I188V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10529365:10529365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454C>A
AA Mutation	p.Leu152Met(p.L152M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10529749:10529749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838G>T
AA Mutation	p.Asp280Tyr(p.D280Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379597
Start	10529208:10529208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379597
Start	10529217:10529217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753973035
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000379597
Start	10621408:10621408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983G>A
AA Mutation	p.Trp328Ter(p.W328*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379597
Start	10529065:10529066(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.159dupT
AA Mutation	p.Glu54Ter(p.E54*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379597
Start	10626601:10626602(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1203_1204insA
AA Mutation	p.Phe402IlefsTer6(p.F402Ifs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GCNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379597
Start	10529612:10529612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701A>G
AA Mutation	p.Gln234Arg(p.Q234R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379597
Start	10529739:10529739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000379597
Start	10529149:10529149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745726583
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Ter(p.R80*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript