Colon Cancer: Gene >> MGAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180791806:180791806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368412689
CDS Mutation	c.1166C>T
AA Mutation	p.Thr389Met(p.T389M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180792515:180792515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765702663
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	ENST00000307826
Start	180792052:180792052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920A>C
AA Mutation	p.Glu307Ala(p.E307A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180791842:180791842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130A>G
AA Mutation	p.Asp377Gly(p.D377G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180792193:180792193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769149714
CDS Mutation	c.779G>A
AA Mutation	p.Arg260His(p.R260H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180792349:180792349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623T>A
AA Mutation	p.Val208Glu(p.V208E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180792521:180792521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180792830:180792830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778419570
CDS Mutation	c.142G>A
AA Mutation	p.Ala48Thr(p.A48T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180791893:180791893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1079C>T
AA Mutation	p.Ala360Val(p.A360V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307826
Start	180791676:180791676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773672393
CDS Mutation	c.1296G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307826
Start	180792501:180792501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769351710
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307826
Start	180792189:180792189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758825004
CDS Mutation	c.783C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307826
Start	180791781:180791781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201677887
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307826
Start	180792357:180792357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307826
Start	180792291:180792291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748284811
CDS Mutation	c.681G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MGAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180791983:180791983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761737308
CDS Mutation	c.989A>G
AA Mutation	p.Lys330Arg(p.K330R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180792025:180792025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316His(p.R316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307826
Start	180792553:180792553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419G>A
AA Mutation	p.Ser140Asn(p.S140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript