Colon Cancer: Gene >> CYP4F22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269703
Start	15551316:15551316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1441G>A
AA Mutation	p.Ala481Thr(p.A481T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269703
Start	15540571:15540571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144569785
CDS Mutation	c.793C>T
AA Mutation	p.Arg265Trp(p.R265W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269703
Start	15529786:15529786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>T
AA Mutation	p.Met100Ile(p.M100I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269703
Start	15525386:15525386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773295754
CDS Mutation	c.50C>T
AA Mutation	p.Thr17Met(p.T17M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269703
Start	15537638:15537638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525C>G
AA Mutation	p.Phe175Leu(p.F175L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269703
Start	15551422:15551422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1547C>T
AA Mutation	p.Thr516Met(p.T516M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269703
Start	15544175:15544175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1032C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269703
Start	15551372:15551372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1497C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269703
Start	15549142:15549142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269703
Start	15537389:15537389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000269703
Start	15540660:15540660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.882G>A
AA Mutation	p.Trp294Ter(p.W294*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYP4F22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269703
Start	15537647:15537647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.534C>A
AA Mutation	p.Ser178Arg(p.S178R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269703
Start	15529725:15529725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116743462
CDS Mutation	c.239C>T
AA Mutation	p.Ala80Val(p.A80V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000269703
Start	15550679:15550679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1341C>A
AA Mutation	p.Tyr447Ter(p.Y447*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript