Colon Cancer: Gene >> TRIO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14316703:14316703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1691A>G
AA Mutation	p.Gln564Arg(p.Q564R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14330791:14330791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1745T>A
AA Mutation	p.Ile582Asn(p.I582N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14336645:14336645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753710560
CDS Mutation	c.1964G>A
AA Mutation	p.Arg655Gln(p.R655Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14287035:14287035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512A>C
AA Mutation	p.Asn171Thr(p.N171T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14336662:14336662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1981C>T
AA Mutation	p.Arg661Trp(p.R661W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14476940:14476940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6130C>A
AA Mutation	p.Leu2044Ile(p.L2044I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14368837:14368837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3004A>G
AA Mutation	p.Lys1002Glu(p.K1002E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14399061:14399061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4605C>A
AA Mutation	p.Ser1535Arg(p.S1535R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14286914:14286914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Cys(p.R131C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14465616:14465616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5739T>G
AA Mutation	p.Ile1913Met(p.I1913M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14358220:14358220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2089G>A
AA Mutation	p.Asp697Asn(p.D697N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14316672:14316672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660A>G
AA Mutation	p.Ile554Val(p.I554V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14481586:14481586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6433A>G
AA Mutation	p.Met2145Val(p.M2145V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14508346:14508346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9218G>A
AA Mutation	p.Arg3073His(p.R3073H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14508003:14508003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780863165
CDS Mutation	c.8875G>A
AA Mutation	p.Ala2959Thr(p.A2959T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14369468:14369468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3161A>C
AA Mutation	p.Asp1054Ala(p.D1054A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14487940:14487940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7312C>T
AA Mutation	p.Arg2438Cys(p.R2438C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14316693:14316693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761067835
CDS Mutation	c.1681C>T
AA Mutation	p.Arg561Trp(p.R561W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14363820:14363820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370634993
CDS Mutation	c.2480G>A
AA Mutation	p.Arg827His(p.R827H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14363853:14363853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2513T>C
AA Mutation	p.Met838Thr(p.M838T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14471330:14471330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5776C>T
AA Mutation	p.Arg1926Cys(p.R1926C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14504524:14504524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8543A>G
AA Mutation	p.Gln2848Arg(p.Q2848R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14374299:14374299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3287C>A
AA Mutation	p.Pro1096Gln(p.P1096Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14401012:14401012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4664T>C
AA Mutation	p.Phe1555Ser(p.F1555S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14485236:14485236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6825T>A
AA Mutation	p.Asn2275Lys(p.N2275K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14270856:14270856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189G>A
AA Mutation	p.Met63Ile(p.M63I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14389293:14389293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3953A>T
AA Mutation	p.Tyr1318Phe(p.Y1318F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14461022:14461022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5207C>T
AA Mutation	p.Ser1736Leu(p.S1736L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14369465:14369465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754511053
CDS Mutation	c.3158C>T
AA Mutation	p.Thr1053Met(p.T1053M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14488201:14488201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7573C>T
AA Mutation	p.Arg2525Cys(p.R2525C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14508206:14508206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200447498
CDS Mutation	c.9078C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14358231:14358231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2100C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14358222:14358222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778327240
CDS Mutation	c.2091C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14488020:14488020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7392G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14374312:14374312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3300G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14387497:14387497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14508233:14508233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369006273
CDS Mutation	c.9105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14297191:14297191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141998293
CDS Mutation	c.1296G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14508092:14508092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55898643
CDS Mutation	c.8964C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14487510:14487510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6882C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14394100:14394100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4281G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14508023:14508023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546106927
CDS Mutation	c.8895C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14479341:14479341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6234C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14508002:14508002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572269818
CDS Mutation	c.8874C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344204
Start	14387518:14387518(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3657delA
AA Mutation	p.Lys1219AsnfsTer43(p.K1219Nfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344204
Start	14487672:14487672(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746654944
CDS Mutation	c.7050delC
AA Mutation	p.Val2351CysfsTer62(p.V2351Cfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344204
Start	14270832:14270832(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.170delA
AA Mutation	p.Asn57ThrfsTer4(p.N57Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	48
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344204
Start	14369389:14369389(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3082delG
AA Mutation	p.Glu1028ArgfsTer29(p.E1028Rfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	49
Mutation Consequence	stop_gained
Transcription ID	ENST00000344204
Start	14387792:14387792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3826C>T
AA Mutation	p.Arg1276Ter(p.R1276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	50
Mutation Consequence	stop_gained
Transcription ID	ENST00000344204
Start	14488114:14488114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7486C>T
AA Mutation	p.Arg2496Ter(p.R2496*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	51
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000344204
Start	14465543:14465543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5668-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TRIO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344204
Start	14336662:14336662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1981C>T
AA Mutation	p.Arg661Trp(p.R661W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14363788:14363788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758409767
CDS Mutation	c.2448C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14291015:14291015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.840G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14462838:14462838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146544278
CDS Mutation	c.5580C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14419819:14419819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5001C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14290946:14290946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344204
Start	14508002:14508002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572269818
CDS Mutation	c.8874C>T
Mutation Classification	Silent
Feature Type	Transcript