Colon Cancer: Gene >> SLC22A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366963
Start	160134034:160134034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748G>A
AA Mutation	p.Ala250Thr(p.A250T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366963
Start	160122071:160122071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136C>T
AA Mutation	p.Pro46Ser(p.P46S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366963
Start	160154847:160154847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1435A>G
AA Mutation	p.Ile479Val(p.I479V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366963
Start	160139787:160139787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777687557
CDS Mutation	c.1196G>A
AA Mutation	p.Arg399His(p.R399H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366963
Start	160130162:160130162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778547168
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366963
Start	160143645:160143645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34295611
CDS Mutation	c.1381G>A
AA Mutation	p.Val461Ile(p.V461I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366963
Start	160143644:160143644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141274044
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366963
Start	160136245:160136245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366963
Start	160134114:160134114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366963
Start	160139851:160139851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260G>T
AA Mutation	p.Met420Ile(p.M420I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript