Colon Cancer: Gene >> ALOX15B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8048545:8048545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2011G>A
AA Mutation	p.Glu671Lys(p.E671K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8048446:8048446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747632525
CDS Mutation	c.1912G>A
AA Mutation	p.Ala638Thr(p.A638T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8044863:8044863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.711C>A
AA Mutation	p.Phe237Leu(p.F237L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8045317:8045317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>A
AA Mutation	p.Ser310Tyr(p.S310Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000380183
Start	8047075:8047075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577207398
CDS Mutation	c.1456C>T
AA Mutation	p.Arg486Cys(p.R486C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8046950:8046950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331G>A
AA Mutation	p.Arg444Lys(p.R444K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000380183
Start	8039388:8039388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150G>T
AA Mutation	p.Glu50Asp(p.E50D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8042821:8042821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>T
AA Mutation	p.Gly205Trp(p.G205W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8045601:8045601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372320255
CDS Mutation	c.1115C>T
AA Mutation	p.Thr372Met(p.T372M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8047896:8047896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1832G>A
AA Mutation	p.Ser611Asn(p.S611N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8047000:8047000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753001193
CDS Mutation	c.1381C>T
AA Mutation	p.Arg461Trp(p.R461W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380183
Start	8039442:8039442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380183
Start	8046990:8046990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1371T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380183
Start	8047753:8047753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1689C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380183
Start	8039254:8039254(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747925269
CDS Mutation	c.104delC
AA Mutation	p.Pro35HisfsTer21(p.P35Hfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ALOX15B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380183
Start	8044915:8044915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763C>A
AA Mutation	p.His255Asn(p.H255N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript