Colon Cancer: Gene >> CYP4A11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46932821:46932821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199678286
CDS Mutation	c.1304G>A
AA Mutation	p.Arg435His(p.R435H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46941412:46941412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22C>A
AA Mutation	p.Pro8Thr(p.P8T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46932789:46932789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556756716
CDS Mutation	c.1336G>A
AA Mutation	p.Ala446Thr(p.A446T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46934458:46934458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892G>C
AA Mutation	p.Ala298Pro(p.A298P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46935108:46935108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>T
AA Mutation	p.Val228Phe(p.V228F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46932810:46932810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315G>A
AA Mutation	p.Gly439Ser(p.G439S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46933988:46933988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180A>G
AA Mutation	p.Ser394Gly(p.S394G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310638
Start	46930124:46930124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1551C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310638
Start	46935013:46935013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310638
Start	46937342:46937342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374742385
CDS Mutation	c.342G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP4A11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46938039:46938039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>C
AA Mutation	p.Gln98His(p.Q98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46941349:46941349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>A
AA Mutation	p.Leu29Met(p.L29M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310638
Start	46935108:46935108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>T
AA Mutation	p.Val228Phe(p.V228F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript