Colon Cancer: Gene >> ALOX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45428748:45428748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965T>C
AA Mutation	p.Val322Ala(p.V322A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45412228:45412228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Asp157Asn(p.D157N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45440560:45440560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371Gln(p.R371Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45443776:45443776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1622C>A
AA Mutation	p.Thr541Asn(p.T541N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45424085:45424085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599C>A
AA Mutation	p.Ser200Tyr(p.S200Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45443099:45443099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1334C>T
AA Mutation	p.Thr445Ile(p.T445I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45428636:45428636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767991624
CDS Mutation	c.853G>A
AA Mutation	p.Val285Met(p.V285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45443812:45443812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1658C>T
AA Mutation	p.Ala553Val(p.A553V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45395903:45395903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148401371
CDS Mutation	c.398G>A
AA Mutation	p.Arg133His(p.R133H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45445667:45445667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2005C>T
AA Mutation	p.Pro669Ser(p.P669S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45445523:45445523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1861T>C
AA Mutation	p.Tyr621His(p.Y621H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45443751:45443751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597C>T
AA Mutation	p.Arg533Trp(p.R533W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374391
Start	45382656:45382656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374391
Start	45382650:45382650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150281723
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374391
Start	45412215:45412215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374391
Start	45412245:45412245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374391
Start	45382494:45382494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764154625
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374391
Start	45382521:45382521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747497283
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374391
Start	45440597:45440597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1149delG
AA Mutation	p.Met383IlefsTer19(p.M383Ifs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000374391
Start	45395908:45395908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>T
AA Mutation	p.Glu135Ter(p.E135*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000374391
Start	45440599:45440601(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1151_1153delACC
AA Mutation	p.Tyr384_Arg385delinsCys(p.Y384_R385delinsC)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ALOX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45382522:45382522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143978950
CDS Mutation	c.190G>A
AA Mutation	p.Glu64Lys(p.E64K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374391
Start	45445578:45445578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754256319
CDS Mutation	c.1916G>A
AA Mutation	p.Arg639His(p.R639H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript