Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CASZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10647988:10647988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201167368
CDS Mutation	c.3310G>A
AA Mutation	p.Ala1104Thr(p.A1104T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10660405:10660405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637T>C
AA Mutation	p.Ser213Pro(p.S213P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10639820:10639820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4402T>C
AA Mutation	p.Phe1468Leu(p.F1468L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10655761:10655761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1553G>A
AA Mutation	p.Arg518His(p.R518H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10646222:10646222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3602C>T
AA Mutation	p.Ser1201Phe(p.S1201F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10646180:10646180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3644A>G
AA Mutation	p.Asn1215Ser(p.N1215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10639188:10639188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5034G>C
AA Mutation	p.Glu1678Asp(p.E1678D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377022
Start	10642999:10642999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4022G>C
AA Mutation	p.Gly1341Ala(p.G1341A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10643263:10643263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3917G>A
AA Mutation	p.Gly1306Asp(p.G1306D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10660455:10660455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587C>T
AA Mutation	p.Thr196Met(p.T196M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10665223:10665223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365A>G
AA Mutation	p.Tyr122Cys(p.Y122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10665355:10665355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376050510
CDS Mutation	c.233G>A
AA Mutation	p.Arg78His(p.R78H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10653977:10653977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2080C>T
AA Mutation	p.Arg694Cys(p.R694C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10639910:10639910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375316064
CDS Mutation	c.4312G>A
AA Mutation	p.Asp1438Asn(p.D1438N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10653934:10653934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768854834
CDS Mutation	c.2123C>T
AA Mutation	p.Ser708Leu(p.S708L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10655767:10655767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>G
AA Mutation	p.Lys516Arg(p.K516R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10665133:10665133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576863717
CDS Mutation	c.455A>T
AA Mutation	p.Asp152Val(p.D152V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10639840:10639840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747304331
CDS Mutation	c.4382G>A
AA Mutation	p.Arg1461His(p.R1461H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10648054:10648054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3244A>G
AA Mutation	p.Met1082Val(p.M1082V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10659774:10659774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268A>T
AA Mutation	p.Asn423Ile(p.N423I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10648035:10648035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538567404
CDS Mutation	c.3263C>T
AA Mutation	p.Pro1088Leu(p.P1088L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10660510:10660510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532G>A
AA Mutation	p.Ala178Thr(p.A178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10659958:10659958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084G>A
AA Mutation	p.Ala362Thr(p.A362T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10655759:10655759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1555G>A
AA Mutation	p.Asp519Asn(p.D519N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10643176:10643176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531901811
CDS Mutation	c.4004G>A
AA Mutation	p.Arg1335His(p.R1335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10660341:10660341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701C>T
AA Mutation	p.Ala234Val(p.A234V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10645010:10645010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3775C>T
AA Mutation	p.Leu1259Phe(p.L1259F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10649367:10649367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569836726
CDS Mutation	c.2951C>T
AA Mutation	p.Ala984Val(p.A984V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10655706:10655706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768005008
CDS Mutation	c.1608C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10639806:10639806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4416G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10651003:10651003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765472382
CDS Mutation	c.2754C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10654433:10654433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139059853
CDS Mutation	c.1824G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10639515:10639515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558077733
CDS Mutation	c.4707G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10660409:10660409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374277022
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10646269:10646269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10653798:10653798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147506563
CDS Mutation	c.2259C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10649108:10649108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3120G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10660511:10660511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10660493:10660493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756337353
CDS Mutation	c.549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377022
Start	10646251:10646251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3573delC
AA Mutation	p.Tyr1191Ter(p.Y1191*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000377022
Start	10645076:10645076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370332553
CDS Mutation	c.3709C>T
AA Mutation	p.Arg1237Ter(p.R1237*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CASZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10665161:10665161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427G>C
AA Mutation	p.Gly143Arg(p.G143R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10653887:10653887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2170G>A
AA Mutation	p.Asp724Asn(p.D724N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10660050:10660050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992G>A
AA Mutation	p.Ser331Asn(p.S331N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10653866:10653866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2191C>A
AA Mutation	p.Leu731Met(p.L731M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10654495:10654495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775345608
CDS Mutation	c.1762C>T
AA Mutation	p.Arg588Cys(p.R588C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377022
Start	10649333:10649333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2985G>T
AA Mutation	p.Lys995Asn(p.K995N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377022
Start	10649111:10649111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3117C>T
Mutation Classification	Silent
Feature Type	Transcript