Mutation

Primary Site >> Stomach Cancer

Gene >> KIF26B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245686498:245686498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780936718
CDS Mutation	c.3515C>T
AA Mutation	p.Thr1172Met(p.T1172M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245687877:245687877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4894G>A
AA Mutation	p.Ala1632Thr(p.A1632T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245698286:245698286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368463171
CDS Mutation	c.6005G>A
AA Mutation	p.Arg2002Gln(p.R2002Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245686320:245686320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182167022
CDS Mutation	c.3337G>A
AA Mutation	p.Val1113Met(p.V1113M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245685814:245685814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762130575
CDS Mutation	c.2831G>A
AA Mutation	p.Ser944Asn(p.S944N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245685579:245685579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2596A>G
AA Mutation	p.Ile866Val(p.I866V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245686419:245686419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3436G>T
AA Mutation	p.Gly1146Trp(p.G1146W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245540810:245540810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Trp(p.R404W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245698891:245698891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6032C>T
AA Mutation	p.Ala2011Val(p.A2011V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245698258:245698258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5977G>A
AA Mutation	p.Glu1993Lys(p.E1993K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245607694:245607694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1601T>C
AA Mutation	p.Val534Ala(p.V534A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245686251:245686251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3268A>G
AA Mutation	p.Lys1090Glu(p.K1090E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245687109:245687109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4126G>A
AA Mutation	p.Ala1376Thr(p.A1376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245687340:245687340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4357G>A
AA Mutation	p.Ala1453Thr(p.A1453T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245646249:245646249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2227C>T
AA Mutation	p.Leu743Phe(p.L743F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245684259:245684259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2285G>T
AA Mutation	p.Arg762Leu(p.R762L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245686440:245686440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs73127009
CDS Mutation	c.3457G>A
AA Mutation	p.Asp1153Asn(p.D1153N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245685553:245685553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2570G>A
AA Mutation	p.Ser857Asn(p.S857N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245686597:245686597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3614G>A
AA Mutation	p.Gly1205Asp(p.G1205D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245602754:245602754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528G>A
AA Mutation	p.Asp510Asn(p.D510N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245688756:245688756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5773G>A
AA Mutation	p.Val1925Met(p.V1925M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000407071
Start	245419745:245419745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767081137
CDS Mutation	c.1166G>A
AA Mutation	p.Arg389Gln(p.R389Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245686786:245686786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3803C>T
AA Mutation	p.Ala1268Val(p.A1268V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245686867:245686867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3884G>A
AA Mutation	p.Cys1295Tyr(p.C1295Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000407071
Start	245698118:245698118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5837G>T
AA Mutation	p.Arg1946Leu(p.R1946L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245611855:245611855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377322149
CDS Mutation	c.1977C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245687303:245687303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775806023
CDS Mutation	c.4320G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245686319:245686319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756197287
CDS Mutation	c.3336C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245602673:245602673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1447T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245688302:245688302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5319G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245685686:245685686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769516810
CDS Mutation	c.2703C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245540773:245540773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245685794:245685794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145851394
CDS Mutation	c.2811C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245540938:245540938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245419704:245419704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245687048:245687048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4065C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245540824:245540824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407071
Start	245609471:245609471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407071
Start	245686177:245686177(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3199delC
AA Mutation	p.Arg1067GlyfsTer65(p.R1067Gfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407071
Start	245684303:245684303(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2329delC
AA Mutation	p.His777ThrfsTer23(p.H777Tfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000407071
Start	245685672:245685672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2689C>T
AA Mutation	p.Gln897Ter(p.Q897*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	stop_gained
Transcription ID	ENST00000407071
Start	245685732:245685732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2749G>T
AA Mutation	p.Glu917Ter(p.E917*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407071
Start	245686605:245686606(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3624dupC
AA Mutation	p.Ser1209GlnfsTer58(p.S1209Qfs*58)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript