Colon Cancer: Gene >> SLC1A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234256
Start	65016537:65016537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755218346
CDS Mutation	c.898G>A
AA Mutation	p.Ala300Thr(p.A300T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234256
Start	65018118:65018118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082G>A
AA Mutation	p.Gly361Asp(p.G361D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234256
Start	65018165:65018165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760189211
CDS Mutation	c.1129G>A
AA Mutation	p.Val377Met(p.V377M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000234256
Start	65020922:65020922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1375A>G
AA Mutation	p.Thr459Ala(p.T459A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000234256
Start	65021006:65021006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1459C>A
AA Mutation	p.Gln487Lys(p.Q487K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234256
Start	65016482:65016482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369182463
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234256
Start	65016536:65016536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561750338
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234256
Start	65018660:65018660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1345C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000234256
Start	65018543:65018543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1230-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC1A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234256
Start	65016447:65016447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808C>T
AA Mutation	p.Pro270Ser(p.P270S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript