Colon Cancer: Gene >> CYP4B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46799232:46799232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151A>G
AA Mutation	p.Thr51Ala(p.T51A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46815235:46815235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1041G>T
AA Mutation	p.Glu347Asp(p.E347D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46818160:46818160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299G>T
AA Mutation	p.Glu433Asp(p.E433D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46799220:46799220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139C>A
AA Mutation	p.Pro47Thr(p.P47T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46813549:46813549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752316206
CDS Mutation	c.563C>T
AA Mutation	p.Ala188Val(p.A188V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46818696:46818696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143680556
CDS Mutation	c.1418G>A
AA Mutation	p.Arg473His(p.R473H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46812520:46812520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392G>T
AA Mutation	p.Gly131Val(p.G131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46814022:46814022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139993247
CDS Mutation	c.731G>A
AA Mutation	p.Arg244His(p.R244H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46814281:46814281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845A>C
AA Mutation	p.His282Pro(p.H282P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46813510:46813510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524G>A
AA Mutation	p.Gly175Asp(p.G175D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46814024:46814024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200200785
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Cys(p.R245C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46813593:46813593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607G>T
AA Mutation	p.Gly203Cys(p.G203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271153
Start	46817993:46817993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271153
Start	46812584:46812584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000271153
Start	46799262:46799262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CYP4B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46815171:46815171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755652341
CDS Mutation	c.977G>T
AA Mutation	p.Trp326Leu(p.W326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271153
Start	46818160:46818160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299G>T
AA Mutation	p.Glu433Asp(p.E433D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271153
Start	46817084:46817084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271153
Start	46815232:46815232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762334759
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript