Colon Cancer: Gene >> SLCO4A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62669011:62669011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958G>T
AA Mutation	p.Gly653Val(p.G653V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62666548:62666548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763020976
CDS Mutation	c.1445C>T
AA Mutation	p.Ala482Val(p.A482V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62668538:62668538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1873C>G
AA Mutation	p.Leu625Val(p.L625V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62668497:62668497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611Lys(p.R611K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62657104:62657104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567670164
CDS Mutation	c.650C>T
AA Mutation	p.Ala217Val(p.A217V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62668485:62668485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368075379
CDS Mutation	c.1820G>A
AA Mutation	p.Arg607His(p.R607H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62668120:62668120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1747T>A
AA Mutation	p.Phe583Ile(p.F583I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62657010:62657010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556G>A
AA Mutation	p.Val186Met(p.V186M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62668064:62668064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1691A>G
AA Mutation	p.His564Arg(p.H564R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62667801:62667801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1529G>A
AA Mutation	p.Cys510Tyr(p.C510Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62667769:62667769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1497C>A
AA Mutation	p.Asn499Lys(p.N499K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217159
Start	62656964:62656964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200742188
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217159
Start	62666393:62666393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1290G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217159
Start	62657042:62657042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217159
Start	62656658:62656658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542833541
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217159
Start	62658708:62658708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLCO4A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217159
Start	62656823:62656823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369C>A
AA Mutation	p.Phe123Leu(p.F123L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript