Colon Cancer: Gene >> SLC1A3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265113
Start	36629585:36629585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317C>T
AA Mutation	p.Thr106Ile(p.T106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36686121:36686121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1481T>C
AA Mutation	p.Val494Ala(p.V494A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36680477:36680477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549250283
CDS Mutation	c.1177G>A
AA Mutation	p.Val393Ile(p.V393I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36676947:36676947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778074144
CDS Mutation	c.623C>T
AA Mutation	p.Thr208Met(p.T208M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36680444:36680444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199787096
CDS Mutation	c.1144G>A
AA Mutation	p.Val382Met(p.V382M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36629548:36629548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.280A>G
AA Mutation	p.Met94Val(p.M94V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36679790:36679790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024C>T
AA Mutation	p.Arg342Trp(p.R342W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36608562:36608562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Trp(p.R47W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36686075:36686075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Trp(p.R479W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36679787:36679787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1021A>G
AA Mutation	p.Thr341Ala(p.T341A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36680468:36680468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1168G>A
AA Mutation	p.Val390Met(p.V390M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265113
Start	36680455:36680455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371866521
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265113
Start	36680569:36680569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758802146
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265113
Start	36679719:36679720(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.953_954insAGAAATTT
AA Mutation	p.Val319GlufsTer4(p.V319Efs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC1A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36629534:36629534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266T>G
AA Mutation	p.Met89Arg(p.M89R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36677142:36677142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.818C>A
AA Mutation	p.Ser273Tyr(p.S273Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36680444:36680444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199787096
CDS Mutation	c.1144G>A
AA Mutation	p.Val382Met(p.V382M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265113
Start	36683982:36683982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750317354
CDS Mutation	c.1408G>A
AA Mutation	p.Ala470Thr(p.A470T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265113
Start	36680467:36680467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372548093
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265113
Start	36679846:36679846(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1083delG
AA Mutation	p.Thr362ProfsTer32(p.T362Pfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000265113
Start	36671073:36671073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Ter(p.R122*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript