Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TCF20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42214701:42214701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605C>T
AA Mutation	p.Ala202Val(p.A202V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42213109:42213109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2197A>G
AA Mutation	p.Lys733Glu(p.K733E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42211285:42211285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4021A>G
AA Mutation	p.Ile1341Val(p.I1341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42212422:42212422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2884C>A
AA Mutation	p.Arg962Ser(p.R962S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42213526:42213526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375607848
CDS Mutation	c.1780G>A
AA Mutation	p.Asp594Asn(p.D594N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42213531:42213531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1775C>T
AA Mutation	p.Ser592Leu(p.S592L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42213580:42213580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765913677
CDS Mutation	c.1726G>A
AA Mutation	p.Ala576Thr(p.A576T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42210678:42210678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4628C>T
AA Mutation	p.Pro1543Leu(p.P1543L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42211417:42211417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3889A>G
AA Mutation	p.Asn1297Asp(p.N1297D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42215107:42215107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Ala67Thr(p.A67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42214465:42214465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>T
AA Mutation	p.Ala281Ser(p.A281S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42179623:42179623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5735G>A
AA Mutation	p.Cys1912Tyr(p.C1912Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42211204:42211204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143492270
CDS Mutation	c.4102G>A
AA Mutation	p.Ala1368Thr(p.A1368T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42212541:42212541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2765A>T
AA Mutation	p.Lys922Ile(p.K922I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42213222:42213222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2084G>A
AA Mutation	p.Arg695Lys(p.R695K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42210549:42210549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4757G>T
AA Mutation	p.Arg1586Ile(p.R1586I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42210748:42210748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4558A>C
AA Mutation	p.Thr1520Pro(p.T1520P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42212602:42212602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2704C>T
AA Mutation	p.Pro902Ser(p.P902S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359486
Start	42214595:42214595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359486
Start	42214022:42214022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359486
Start	42212909:42212909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2397T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359486
Start	42210257:42210257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138453240
CDS Mutation	c.5049G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359486
Start	42214538:42214538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42212223:42212223(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3083delG
AA Mutation	p.Gly1028GlufsTer6(p.G1028Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42211143:42211144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4162_4163delTT
AA Mutation	p.Leu1388GlufsTer6(p.L1388Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42214942:42214942(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.364delC
AA Mutation	p.Gln122ArgfsTer62(p.Q122Rfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42213599:42213599(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1707delC
AA Mutation	p.Arg570AspfsTer37(p.R570Dfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42168710:42168710(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780246928
CDS Mutation	c.5826delC
AA Mutation	p.Leu1943CysfsTer118(p.L1943Cfs*118)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42210569:42210569(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4737delA
AA Mutation	p.Lys1579AsnfsTer36(p.K1579Nfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42210624:42210624(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4682delC
AA Mutation	p.Pro1561LeufsTer54(p.P1561Lfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42210133:42210133(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5173delT
AA Mutation	p.Tyr1725IlefsTer157(p.Y1725Ifs*157)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000359486
Start	42211750:42211750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3556G>T
AA Mutation	p.Glu1186Ter(p.E1186*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42211037:42211038(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4265_4268dupAGGA
AA Mutation	p.Leu1424GlyfsTer21(p.L1424Gfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359486
Start	42214941:42214942(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs777979354
CDS Mutation	c.364dupC
AA Mutation	p.Gln122ProfsTer12(p.Q122Pfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000359486
Start	42214566:42214567(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs761310557
CDS Mutation	c.737_739dupCCT
AA Mutation	p.Ser246dup(p.S246dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TCF20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42214394:42214394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912G>T
AA Mutation	p.Lys304Asn(p.K304N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42213644:42213644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1662G>T
AA Mutation	p.Glu554Asp(p.E554D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359486
Start	42214124:42214124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>T
AA Mutation	p.Glu394Asp(p.E394D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359486
Start	42214352:42214352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750872618
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359486
Start	42210737:42210737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142330661
CDS Mutation	c.4569G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359486
Start	42211307:42211307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3999C>T
Mutation Classification	Silent
Feature Type	Transcript