Colon Cancer: Gene >> SLC3A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44280785:44280785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500A>C
AA Mutation	p.Lys167Thr(p.K167T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44320398:44320398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1817A>G
AA Mutation	p.Asn606Ser(p.N606S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44275846:44275846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311C>T
AA Mutation	p.Thr104Ile(p.T104I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44281461:44281461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758636942
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44312727:44312727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201989712
CDS Mutation	c.1474G>A
AA Mutation	p.Ala492Thr(p.A492T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44320241:44320241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660G>T
AA Mutation	p.Asp554Tyr(p.D554Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44281462:44281462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138395881
CDS Mutation	c.686G>A
AA Mutation	p.Arg229Gln(p.R229Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44304186:44304186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780321792
CDS Mutation	c.1180G>A
AA Mutation	p.Val394Met(p.V394M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260649
Start	44312610:44312610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260649
Start	44304173:44304173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1167T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260649
Start	44301050:44301050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371470993
CDS Mutation	c.1059G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260649
Start	44280789:44280789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747172398
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260649
Start	44275616:44275616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260649
Start	44304188:44304188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1182G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC3A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260649
Start	44286068:44286068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757239030
CDS Mutation	c.802G>A
AA Mutation	p.Glu268Lys(p.E268K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript