Mutation

Primary Site >> Stomach Cancer

Gene >> KIF21A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39330781:39330781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3284C>A
AA Mutation	p.Pro1095His(p.P1095H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39330871:39330871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3194T>C
AA Mutation	p.Leu1065Pro(p.L1065P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361418
Start	39309764:39309764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756337041
CDS Mutation	c.4099C>T
AA Mutation	p.Arg1367Cys(p.R1367C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39337100:39337100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2414G>T
AA Mutation	p.Arg805Ile(p.R805I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39357397:39357397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256A>T
AA Mutation	p.Asn419Ile(p.N419I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39332935:39332935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145318959
CDS Mutation	c.2660C>T
AA Mutation	p.Ala887Val(p.A887V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39333228:39333228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558002876
CDS Mutation	c.2471G>A
AA Mutation	p.Arg824His(p.R824H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39301595:39301595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4816G>T
AA Mutation	p.Gly1606Cys(p.G1606C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39369734:39369734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445T>A
AA Mutation	p.Leu149Ile(p.L149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39332673:39332673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2774T>G
AA Mutation	p.Leu925Arg(p.L925R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39357419:39357419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750947190
CDS Mutation	c.1234G>A
AA Mutation	p.Glu412Lys(p.E412K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39322788:39322788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3551G>A
AA Mutation	p.Gly1184Asp(p.G1184D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361418
Start	39332688:39332688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747284586
CDS Mutation	c.2759G>A
AA Mutation	p.Arg920His(p.R920H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361418
Start	39341581:39341581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749121235
CDS Mutation	c.1845G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361418
Start	39358301:39358301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751695880
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361418
Start	39363109:39363109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361418
Start	39341569:39341569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1857G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361418
Start	39311448:39311448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4065T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361418
Start	39309708:39309708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4155T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000361418
Start	39351778:39351778(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1672delA
AA Mutation	p.Arg558GlyfsTer42(p.R558Gfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39369792:39369792(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.387delA
AA Mutation	p.Lys129AsnfsTer3(p.K129Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39319982:39319982(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769295012
CDS Mutation	c.3703delA
AA Mutation	p.Ile1235PhefsTer7(p.I1235Ffs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39340327:39340327(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2148delA
AA Mutation	p.Val717LeufsTer12(p.V717Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39340170:39340170(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2305delA
AA Mutation	p.Thr769GlnfsTer5(p.T769Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39351933:39351933(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1517delA
AA Mutation	p.Asn506ThrfsTer2(p.N506Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39351821:39351821(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1629delA
AA Mutation	p.Asp544IlefsTer2(p.D544Ifs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39332738:39332738(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2709delA
AA Mutation	p.Lys903AsnfsTer7(p.K903Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000361418
Start	39322741:39322741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3598G>T
AA Mutation	p.Glu1200Ter(p.E1200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39340169:39340170(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2305dupA
AA Mutation	p.Thr769AsnfsTer20(p.T769Nfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361418
Start	39369791:39369792(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.387dupA
AA Mutation	p.His130ThrfsTer5(p.H130Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	31
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000361418
Start	39332409:39332409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2857-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript