Colon Cancer: Gene >> SLITRK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676265:87676265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>A
AA Mutation	p.Glu293Lys(p.E293K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677394:87677394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006G>A
AA Mutation	p.Ser669Asn(p.S669N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677295:87677295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1907C>T
AA Mutation	p.Ala636Val(p.A636V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87675705:87675705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317G>C
AA Mutation	p.Gly106Ala(p.G106A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677778:87677778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11840163
CDS Mutation	c.2390A>C
AA Mutation	p.Gln797Pro(p.Q797P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677017:87677017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1629G>T
AA Mutation	p.Leu543Phe(p.L543F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87675443:87675443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55C>T
AA Mutation	p.His19Tyr(p.H19Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677420:87677420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2032G>A
AA Mutation	p.Val678Ile(p.V678I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677395:87677395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2007C>A
AA Mutation	p.Ser669Arg(p.S669R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87675831:87675831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146758652
CDS Mutation	c.443C>A
AA Mutation	p.Thr148Asn(p.T148N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676214:87676214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826G>A
AA Mutation	p.Asp276Asn(p.D276N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87675773:87675773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376984309
CDS Mutation	c.385C>T
AA Mutation	p.Arg129Trp(p.R129W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87675944:87675944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556G>T
AA Mutation	p.Asp186Tyr(p.D186Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677015:87677015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1627T>G
AA Mutation	p.Leu543Val(p.L543V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676603:87676603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1215G>T
AA Mutation	p.Gln405His(p.Q405H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676281:87676281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893C>T
AA Mutation	p.Thr298Met(p.T298M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676424:87676424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036T>C
AA Mutation	p.Ser346Pro(p.S346P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676944:87676944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1556C>T
AA Mutation	p.Ala519Val(p.A519V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87678178:87678178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750330122
CDS Mutation	c.2790C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87675430:87675430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87677182:87677182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555137445
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87677170:87677170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87677161:87677161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1773C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87675934:87675934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87677347:87677347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1959C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87676741:87676741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1353C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87677629:87677629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2241C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87675580:87675580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87677284:87677284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779169011
CDS Mutation	c.1896G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87676039:87676039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325089
Start	87677948:87677948(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2563delT
AA Mutation	p.Tyr855ThrfsTer5(p.Y855Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325089
Start	87678100:87678100(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2716delG
AA Mutation	p.Ala906GlnfsTer20(p.A906Qfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325089
Start	87678079:87678079(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2695delC
AA Mutation	p.His899IlefsTer27(p.H899Ifs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000325089
Start	87676574:87676574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186C>T
AA Mutation	p.Arg396Ter(p.R396*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325089
Start	87676486:87676487(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1101dupA
AA Mutation	p.Ser368IlefsTer19(p.S368Ifs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325089
Start	87676164:87676165(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.781dupG
AA Mutation	p.Asp261GlyfsTer5(p.D261Gfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLITRK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87678179:87678179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2791G>A
AA Mutation	p.Glu931Lys(p.E931K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87675477:87675477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89T>A
AA Mutation	p.Val30Glu(p.V30E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676442:87676442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>T
AA Mutation	p.Asp352Tyr(p.D352Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676141:87676141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753C>A
AA Mutation	p.Asp251Glu(p.D251E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87675589:87675589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201C>A
AA Mutation	p.Asn67Lys(p.N67K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677048:87677048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1660T>C
AA Mutation	p.Ser554Pro(p.S554P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87678127:87678127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2739A>T
AA Mutation	p.Glu913Asp(p.E913D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677127:87677127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1739A>G
AA Mutation	p.Gln580Arg(p.Q580R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677756:87677756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766013136
CDS Mutation	c.2368C>T
AA Mutation	p.His790Tyr(p.H790Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676647:87676647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1259A>C
AA Mutation	p.Tyr420Ser(p.Y420S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677183:87677183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1795G>C
AA Mutation	p.Ala599Pro(p.A599P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676275:87676275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533532510
CDS Mutation	c.887C>T
AA Mutation	p.Pro296Leu(p.P296L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87677198:87677198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371327441
CDS Mutation	c.1810C>T
AA Mutation	p.Arg604Cys(p.R604C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87675672:87675672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370073384
CDS Mutation	c.284G>A
AA Mutation	p.Arg95His(p.R95H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000325089
Start	87676173:87676173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785T>C
AA Mutation	p.Val262Ala(p.V262A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325089
Start	87676286:87676286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898T>C
Mutation Classification	Silent
Feature Type	Transcript