Colon Cancer: Gene >> ALOX15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293761
Start	4637209:4637209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857C>T
AA Mutation	p.Ala286Val(p.A286V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293761
Start	4633219:4633219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763395191
CDS Mutation	c.1345G>A
AA Mutation	p.Asp449Asn(p.D449N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293761
Start	4637204:4637204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760254381
CDS Mutation	c.862G>A
AA Mutation	p.Val288Ile(p.V288I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293761
Start	4635864:4635864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143365387
CDS Mutation	c.1056C>A
AA Mutation	p.Phe352Leu(p.F352L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293761
Start	4631654:4631654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1935C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293761
Start	4637118:4637118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293761
Start	4635885:4635885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201380740
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293761
Start	4637136:4637136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293761
Start	4633468:4633468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761865940
CDS Mutation	c.1194A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293761
Start	4632042:4632042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293761
Start	4631964:4631964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370211925
CDS Mutation	c.1734G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000293761
Start	4631915:4631915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1783C>T
AA Mutation	p.Gln595Ter(p.Q595*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ALOX15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293761
Start	4639496:4639496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139214774
CDS Mutation	c.271G>A
AA Mutation	p.Glu91Lys(p.E91K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293761
Start	4632184:4632184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1638C>G
Mutation Classification	Silent
Feature Type	Transcript