Colon Cancer: Gene >> SLCO2B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289575
Start	75204543:75204543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144746239
CDS Mutation	c.2093C>T
AA Mutation	p.Ser698Leu(p.S698L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289575
Start	75193247:75193247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543049597
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Cys(p.R369C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289575
Start	75204449:75204449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745594123
CDS Mutation	c.1999G>A
AA Mutation	p.Ala667Thr(p.A667T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289575
Start	75169262:75169262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538T>C
AA Mutation	p.Tyr180His(p.Y180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289575
Start	75204565:75204565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2115G>T
AA Mutation	p.Glu705Asp(p.E705D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000289575
Start	75193380:75193380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762752722
CDS Mutation	c.1238T>C
AA Mutation	p.Ile413Thr(p.I413T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289575
Start	75169330:75169330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371064308
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289575
Start	75165858:75165858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289575
Start	75193232:75193232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLCO2B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289575
Start	75169731:75169731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762316212
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Cys(p.R250C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript