Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TET3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74099301:74099301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754481733
CDS Mutation	c.3293A>G
AA Mutation	p.Asn1098Ser(p.N1098S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74048075:74048075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2158G>A
AA Mutation	p.Asp720Asn(p.D720N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74046951:74046951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034G>A
AA Mutation	p.Ser345Asn(p.S345N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74099303:74099303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3295C>T
AA Mutation	p.Arg1099Cys(p.R1099C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74100900:74100900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4112A>G
AA Mutation	p.Lys1371Arg(p.K1371R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74047289:74047289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377755568
CDS Mutation	c.1372G>A
AA Mutation	p.Asp458Asn(p.D458N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74099309:74099309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748561400
CDS Mutation	c.3301G>A
AA Mutation	p.Val1101Met(p.V1101M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74087948:74087948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2798G>A
AA Mutation	p.Arg933His(p.R933H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74087986:74087986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2836A>G
AA Mutation	p.Thr946Ala(p.T946A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74101899:74101899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5111A>G
AA Mutation	p.His1704Arg(p.H1704R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74046507:74046507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590C>T
AA Mutation	p.Ala197Val(p.A197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74046381:74046381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766359553
CDS Mutation	c.464C>T
AA Mutation	p.Pro155Leu(p.P155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74046606:74046606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763917193
CDS Mutation	c.689G>A
AA Mutation	p.Arg230His(p.R230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74099438:74099438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3430G>A
AA Mutation	p.Ala1144Thr(p.A1144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74101728:74101728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4940T>C
AA Mutation	p.Leu1647Pro(p.L1647P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74093580:74093580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3181C>T
AA Mutation	p.Arg1061Trp(p.R1061W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74047857:74047857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940C>A
AA Mutation	p.Pro647His(p.P647H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74102154:74102154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5366G>A
AA Mutation	p.Gly1789Asp(p.G1789D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000409262
Start	74089898:74089898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2890C>T
AA Mutation	p.Arg964Trp(p.R964W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74101680:74101680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761824851
CDS Mutation	c.4892C>T
AA Mutation	p.Ala1631Val(p.A1631V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74047538:74047538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1621G>C
AA Mutation	p.Glu541Gln(p.E541Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74047156:74047156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74046739:74046739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74047951:74047951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2034C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74099308:74099308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779499652
CDS Mutation	c.3300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74101309:74101309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375740189
CDS Mutation	c.4521G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74100556:74100556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752918208
CDS Mutation	c.3768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74101727:74101727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74092946:74092946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373633219
CDS Mutation	c.3084C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74101111:74101111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4323C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74101732:74101732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756777520
CDS Mutation	c.4944C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74100936:74100936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4152delC
AA Mutation	p.Phe1385LeufsTer17(p.F1385Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74102025:74102025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5243delG
AA Mutation	p.Gly1748AlafsTer106(p.G1748Afs*106)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74101634:74101634(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4851delC
AA Mutation	p.Ser1618AlafsTer5(p.S1618Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74048203:74048203(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2290delG
AA Mutation	p.Ala764LeufsTer2(p.A764Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74047047:74047047(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1135delC
AA Mutation	p.Gln379ArgfsTer162(p.Q379Rfs*162)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74101214:74101214(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4429delG
AA Mutation	p.Ala1477ProfsTer54(p.A1477Pfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74048095:74048095(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2183delC
AA Mutation	p.Pro728LeufsTer38(p.P728Lfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000409262
Start	74101313:74101313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4525C>T
AA Mutation	p.Arg1509Ter(p.R1509*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74102024:74102025(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs759623160
CDS Mutation	c.5243dupG
AA Mutation	p.Thr1749HisfsTer5(p.T1749Hfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409262
Start	74100510:74100511(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3724dupG
AA Mutation	p.Val1242GlyfsTer44(p.V1242Gfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000409262
Start	74099541:74099543(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3535_3537delGAG
AA Mutation	p.Glu1179del(p.E1179del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TET3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74048052:74048052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs57955681
CDS Mutation	c.2135G>A
AA Mutation	p.Arg712Gln(p.R712Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74101314:74101314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201185906
CDS Mutation	c.4526G>A
AA Mutation	p.Arg1509Gln(p.R1509Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409262
Start	74047502:74047502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1585C>A
AA Mutation	p.Gln529Lys(p.Q529K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409262
Start	74046667:74046667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript