Colon Cancer: Gene >> SLC38A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614032
Start	50217469:50217469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780109786
CDS Mutation	c.686T>C
AA Mutation	p.Ile229Thr(p.I229T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000614032
Start	50218279:50218279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945G>T
AA Mutation	p.Lys315Asn(p.K315N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000614032
Start	50218361:50218361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027A>G
AA Mutation	p.Thr343Ala(p.T343A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000614032
Start	50218862:50218862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220A>G
AA Mutation	p.His407Arg(p.H407R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000614032
Start	50214434:50214434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.134G>A
AA Mutation	p.Gly45Asp(p.G45D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000614032
Start	50214278:50214278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79A>G
AA Mutation	p.Thr27Ala(p.T27A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000614032
Start	50215816:50215816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543A>C
AA Mutation	p.Lys181Asn(p.K181N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614032
Start	50218902:50218902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614032
Start	50220156:50220156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1494C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614032
Start	50215632:50215632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774193705
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614032
Start	50219971:50219971(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1401delC
AA Mutation	p.Ile469SerfsTer13(p.I469Sfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000614032
Start	50218822:50218822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1180C>T
AA Mutation	p.Gln394Ter(p.Q394*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC38A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614032
Start	50215405:50215405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780657967
CDS Mutation	c.319G>A
AA Mutation	p.Ala107Thr(p.A107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614032
Start	50217684:50217684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614032
Start	50218642:50218642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1086T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614032
Start	50218297:50218297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.963C>A
Mutation Classification	Silent
Feature Type	Transcript