Colon Cancer: Gene >> MGAT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488935:39488935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751551105
CDS Mutation	c.1588G>A
AA Mutation	p.Glu530Lys(p.E530K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39487675:39487675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760106779
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Cys(p.R110C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488143:39488143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Cys(p.R266C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488092:39488092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Trp(p.R249W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488153:39488153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.806T>C
AA Mutation	p.Val269Ala(p.V269A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488725:39488725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378C>T
AA Mutation	p.Arg460Cys(p.R460C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488746:39488746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376388006
CDS Mutation	c.1399G>A
AA Mutation	p.Gly467Ser(p.G467S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488888:39488888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541G>A
AA Mutation	p.Arg514His(p.R514H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39487517:39487517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170C>T
AA Mutation	p.Thr57Met(p.T57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488192:39488192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845G>T
AA Mutation	p.Arg282Leu(p.R282L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488356:39488356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009A>G
AA Mutation	p.Thr337Ala(p.T337A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39488126:39488126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779G>A
AA Mutation	p.Gly260Asp(p.G260D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39487672:39487672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Val109Met(p.V109M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000341184
Start	39487795:39487795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776299748
CDS Mutation	c.448C>T
AA Mutation	p.Arg150Trp(p.R150W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341184
Start	39488001:39488001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341184
Start	39488661:39488661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1314C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341184
Start	39487446:39487446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341184
Start	39488013:39488013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341184
Start	39487893:39487893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770523032
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000341184
Start	39487540:39487540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193G>T
AA Mutation	p.Gly65Ter(p.G65*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MGAT3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341184
Start	39487614:39487614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341184
Start	39488253:39488253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906G>A
Mutation Classification	Silent
Feature Type	Transcript