Colon Cancer: Gene >> SLCO3A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92147000:92147000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747334812
CDS Mutation	c.1529C>T
AA Mutation	p.Ala510Val(p.A510V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92162933:92162933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774889130
CDS Mutation	c.1931C>T
AA Mutation	p.Thr644Met(p.T644M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92128415:92128415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1438G>T
AA Mutation	p.Asp480Tyr(p.D480Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	91854001:91854001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93G>T
AA Mutation	p.Lys31Asn(p.K31N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	91916056:91916056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244G>A
AA Mutation	p.Ala82Thr(p.A82T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92163119:92163119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2117T>C
AA Mutation	p.Met706Thr(p.M706T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92126139:92126139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778480265
CDS Mutation	c.1253T>C
AA Mutation	p.Leu418Pro(p.L418P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92126157:92126157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1271C>T
AA Mutation	p.Ala424Val(p.A424V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	91916074:91916074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Gly88Arg(p.G88R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92104419:92104419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367922921
CDS Mutation	c.886G>A
AA Mutation	p.Ala296Thr(p.A296T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92126141:92126141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255G>C
AA Mutation	p.Gly419Arg(p.G419R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92126102:92126102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216G>A
AA Mutation	p.Gly406Arg(p.G406R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92163055:92163055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762873968
CDS Mutation	c.2053G>A
AA Mutation	p.Ala685Thr(p.A685T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	91916422:91916422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745409648
CDS Mutation	c.610G>A
AA Mutation	p.Asp204Asn(p.D204N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	91916287:91916287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>A
AA Mutation	p.Glu159Lys(p.E159K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92120594:92120594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139T>G
AA Mutation	p.Phe380Cys(p.F380C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92104472:92104472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747216199
CDS Mutation	c.939G>T
AA Mutation	p.Lys313Asn(p.K313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318445
Start	92104448:92104448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367736458
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318445
Start	92104460:92104460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780192633
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318445
Start	92162985:92162985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76755470
CDS Mutation	c.1983C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318445
Start	91916115:91916115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318445
Start	92126188:92126188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318445
Start	92104496:92104496(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.967delC
AA Mutation	p.Leu323TrpfsTer13(p.L323Wfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLCO3A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92147054:92147054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1583C>T
AA Mutation	p.Pro528Leu(p.P528L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318445
Start	92120560:92120560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1105G>A
AA Mutation	p.Ala369Thr(p.A369T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318445
Start	92128420:92128420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1443C>A
Mutation Classification	Silent
Feature Type	Transcript