Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TCERG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146463706:146463706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048C>G
AA Mutation	p.Gln350Glu(p.Q350E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146459286:146459286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841T>C
AA Mutation	p.Ser281Pro(p.S281P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146507126:146507126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2829G>T
AA Mutation	p.Glu943Asp(p.E943D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146507933:146507933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2971A>T
AA Mutation	p.Ile991Phe(p.I991F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146455240:146455240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244C>A
AA Mutation	p.Pro82Thr(p.P82T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146471528:146471528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1553C>A
AA Mutation	p.Ala518Asp(p.A518D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146507166:146507166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2869A>G
AA Mutation	p.Lys957Glu(p.K957E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146510573:146510573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3228T>A
AA Mutation	p.Asp1076Glu(p.D1076E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146509199:146509199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3049G>T
AA Mutation	p.Ala1017Ser(p.A1017S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146492933:146492933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2126A>T
AA Mutation	p.Tyr709Phe(p.Y709F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146509203:146509203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3053A>T
AA Mutation	p.Asp1018Val(p.D1018V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146455112:146455112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116T>C
AA Mutation	p.Val39Ala(p.V39A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146478564:146478564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673G>A
AA Mutation	p.Arg558Gln(p.R558Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146493019:146493019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2212G>A
AA Mutation	p.Glu738Lys(p.E738K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146498573:146498573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2269G>T
AA Mutation	p.Asp757Tyr(p.D757Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146468373:146468373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1168T>C
AA Mutation	p.Tyr390His(p.Y390H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146510540:146510540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3195G>T
AA Mutation	p.Glu1065Asp(p.E1065D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296702
Start	146498545:146498545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2241T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296702
Start	146482676:146482676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1971C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296702
Start	146455191:146455191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769859634
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296702
Start	146468387:146468387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763547220
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296702
Start	146503942:146503943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2675_2676delAG
AA Mutation	p.Glu892AlafsTer17(p.E892Afs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296702
Start	146507160:146507160(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs758822980
CDS Mutation	c.2870delA
AA Mutation	p.Lys957ArgfsTer17(p.K957Rfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296702
Start	146480083:146480083(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1881delA
AA Mutation	p.Lys627AsnfsTer37(p.K627Nfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296702
Start	146507902:146507902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2947delA
AA Mutation	p.Ile983SerfsTer41(p.I983Sfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000296702
Start	146480042:146480042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1834G>T
AA Mutation	p.Glu612Ter(p.E612*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000296702
Start	146503890:146503890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2614C>T
AA Mutation	p.Arg872Ter(p.R872*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000296702
Start	146493037:146493037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2230A>T
AA Mutation	p.Arg744Ter(p.R744*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000296702
Start	146455138:146455138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Ter(p.R48*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296702
Start	146493003:146493004(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2203dupA
AA Mutation	p.Met735AsnfsTer8(p.M735Nfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296702
Start	146507901:146507902(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2947dupA
AA Mutation	p.Ile983AsnfsTer3(p.I983Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TCERG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146482599:146482599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748124301
CDS Mutation	c.1894G>A
AA Mutation	p.Asp632Asn(p.D632N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000296702
Start	146457184:146457184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287G>T
AA Mutation	p.Arg96Ile(p.R96I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146459323:146459323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758260296
CDS Mutation	c.878C>T
AA Mutation	p.Ala293Val(p.A293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296702
Start	146510512:146510512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762326791
CDS Mutation	c.3167G>A
AA Mutation	p.Arg1056Gln(p.R1056Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296702
Start	146458958:146458958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296702
Start	146507902:146507902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2947delA
AA Mutation	p.Ile983SerfsTer41(p.I983Sfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000296702
Start	146507927:146507927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2965C>T
AA Mutation	p.Arg989Ter(p.R989*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000296702
Start	146471497:146471497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1522G>T
AA Mutation	p.Glu508Ter(p.E508*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000296702
Start	146509157:146509157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3007G>T
AA Mutation	p.Glu1003Ter(p.E1003*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000296702
Start	146503429:146503429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2437C>T
AA Mutation	p.Arg813Ter(p.R813*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000296702
Start	146503968:146503968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2692G>T
AA Mutation	p.Glu898Ter(p.E898*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript