Colon Cancer: Gene >> CYP4F11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248041
Start	15914381:15914381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321G>A
AA Mutation	p.Asp441Asn(p.D441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248041
Start	15929478:15929478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138578304
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Trp(p.R108W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248041
Start	15922107:15922107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045G>A
AA Mutation	p.Glu349Lys(p.E349K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000248041
Start	15934309:15934309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367904490
CDS Mutation	c.100G>A
AA Mutation	p.Val34Ile(p.V34I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000248041
Start	15927295:15927295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760671891
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248041
Start	15934244:15934244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775052609
CDS Mutation	c.165G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248041
Start	15934403:15934403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767868619
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP4F11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248041
Start	15927300:15927300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770840051
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248041
Start	15914648:15914648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268A>C
AA Mutation	p.Asn423Thr(p.N423T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248041
Start	15913887:15913887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201156268
CDS Mutation	c.1420G>A
AA Mutation	p.Ala474Thr(p.A474T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript