Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF91

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361610:23361610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369A>T
AA Mutation	p.Thr457Ser(p.T457S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361655:23361655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324G>T
AA Mutation	p.Ala442Ser(p.A442S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23359413:23359413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3566T>G
AA Mutation	p.Leu1189Arg(p.L1189R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23359770:23359770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759787392
CDS Mutation	c.3209G>T
AA Mutation	p.Arg1070Ile(p.R1070I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23362187:23362187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792A>C
AA Mutation	p.Lys264Asn(p.K264N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23360342:23360342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2637G>T
AA Mutation	p.Glu879Asp(p.E879D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361030:23361030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949G>T
AA Mutation	p.Arg650Ile(p.R650I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23362105:23362105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874A>G
AA Mutation	p.Lys292Glu(p.K292E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361172:23361172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1807A>G
AA Mutation	p.Lys603Glu(p.K603E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23362285:23362285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>A
AA Mutation	p.His232Asn(p.H232N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23360925:23360925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2054C>T
AA Mutation	p.Pro685Leu(p.P685L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361240:23361240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1739G>T
AA Mutation	p.Gly580Val(p.G580V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23374751:23374751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44T>A
AA Mutation	p.Phe15Tyr(p.F15Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23362141:23362141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838A>G
AA Mutation	p.Thr280Ala(p.T280A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23359675:23359675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370911694
CDS Mutation	c.3304G>A
AA Mutation	p.Gly1102Arg(p.G1102R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23360311:23360311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774009331
CDS Mutation	c.2668G>A
AA Mutation	p.Ala890Thr(p.A890T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23362132:23362132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847A>G
AA Mutation	p.Arg283Gly(p.R283G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23359830:23359830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3149A>T
AA Mutation	p.Tyr1050Phe(p.Y1050F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23360896:23360896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083T>C
AA Mutation	p.Phe695Leu(p.F695L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23360400:23360400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2579G>A
AA Mutation	p.Gly860Asp(p.G860D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23373819:23373819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176C>A
AA Mutation	p.Pro59Gln(p.P59Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361372:23361372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761559122
CDS Mutation	c.1607A>G
AA Mutation	p.His536Arg(p.H536R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23359779:23359779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3200G>A
AA Mutation	p.Gly1067Glu(p.G1067E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23360356:23360356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2623A>C
AA Mutation	p.Ile875Leu(p.I875L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361940:23361940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039G>A
AA Mutation	p.Glu347Lys(p.E347K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300619
Start	23359466:23359466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369770719
CDS Mutation	c.3513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300619
Start	23360768:23360768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2211T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300619
Start	23360702:23360702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2277A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300619
Start	23359811:23359811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000300619
Start	23359924:23359924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3055G>T
AA Mutation	p.Glu1019Ter(p.E1019*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000300619
Start	23360890:23360890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2089C>T
AA Mutation	p.Arg697Ter(p.R697*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000300619
Start	23361924:23361925(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1054_1055insTTTATGTTTA
AA Mutation	p.Cys352PhefsTer4(p.C352Ffs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300619
Start	23360734:23360735(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2244_2245insTA
AA Mutation	p.Lys749Ter(p.K749*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF91

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23360805:23360805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764441211
CDS Mutation	c.2174G>A
AA Mutation	p.Arg725Gln(p.R725Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361030:23361030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949G>T
AA Mutation	p.Arg650Ile(p.R650I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361150:23361150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1829C>T
AA Mutation	p.Ala610Val(p.A610V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23362045:23362045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934C>T
AA Mutation	p.His312Tyr(p.H312Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361954:23361954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374821944
CDS Mutation	c.1025G>T
AA Mutation	p.Arg342Ile(p.R342I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361030:23361030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949G>A
AA Mutation	p.Arg650Lys(p.R650K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361285:23361285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1694A>C
AA Mutation	p.Lys565Thr(p.K565T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23361534:23361534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1445G>T
AA Mutation	p.Arg482Met(p.R482M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300619
Start	23362671:23362671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.308C>A
AA Mutation	p.Ser103Tyr(p.S103Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000300619
Start	23360323:23360323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2656G>T
AA Mutation	p.Glu886Ter(p.E886*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000300619
Start	23374734:23374734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61G>T
AA Mutation	p.Glu21Ter(p.E21*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript