Colon Cancer: Gene >> MGAT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134254623:134254623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138982519
CDS Mutation	c.220G>A
AA Mutation	p.Ala74Thr(p.A74T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134441785:134441785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1897C>T
AA Mutation	p.Pro633Ser(p.P633S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134254539:134254539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136C>A
AA Mutation	p.Leu46Met(p.L46M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134428401:134428401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1831G>T
AA Mutation	p.Gly611Trp(p.G611W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134317576:134317576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778408120
CDS Mutation	c.454G>A
AA Mutation	p.Gly152Ser(p.G152S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134254542:134254542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Cys(p.R47C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134428422:134428422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1852G>A
AA Mutation	p.Ala618Thr(p.A618T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134270431:134270431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768197190
CDS Mutation	c.287G>A
AA Mutation	p.Arg96His(p.R96H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134422899:134422899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1774A>G
AA Mutation	p.Lys592Glu(p.K592E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134344956:134344956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145359732
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335Gln(p.R335Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134412957:134412957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1619A>G
AA Mutation	p.Asn540Ser(p.N540S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281923
Start	134317569:134317569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767409825
CDS Mutation	c.447T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281923
Start	134448766:134448766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764284751
CDS Mutation	c.2145C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281923
Start	134349874:134349874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772061523
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281923
Start	134318718:134318718(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.558delT
AA Mutation	p.Phe186LeufsTer43(p.F186Lfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281923
Start	134349898:134349898(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1209delA
AA Mutation	p.Lys403AsnfsTer4(p.K403Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000281923
Start	134345015:134345015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063G>T
AA Mutation	p.Gly355Ter(p.G355*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	start_lost
Transcription ID	ENST00000281923
Start	134254405:134254405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MGAT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134412976:134412976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1638A>C
AA Mutation	p.Lys546Asn(p.K546N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134254480:134254480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77G>A
AA Mutation	p.Gly26Asp(p.G26D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript