Mutation

Primary Site >> Stomach Cancer

Gene >> KIF4B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155015414:155015414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555C>A
AA Mutation	p.Gln519Lys(p.Q519K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155016041:155016041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776866601
CDS Mutation	c.2182C>T
AA Mutation	p.Arg728Trp(p.R728W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155016697:155016697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2838G>T
AA Mutation	p.Lys946Asn(p.K946N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155016825:155016825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2966T>C
AA Mutation	p.Ile989Thr(p.I989T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155014749:155014749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890T>C
AA Mutation	p.Leu297Pro(p.L297P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155014773:155014773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914G>A
AA Mutation	p.Ser305Asn(p.S305N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155015751:155015751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778653406
CDS Mutation	c.1892G>A
AA Mutation	p.Arg631His(p.R631H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155014115:155014115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256G>A
AA Mutation	p.Ala86Thr(p.A86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155015153:155015153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778448313
CDS Mutation	c.1294G>A
AA Mutation	p.Ala432Thr(p.A432T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155015814:155015814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199820075
CDS Mutation	c.1955G>A
AA Mutation	p.Arg652His(p.R652H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155014071:155014071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752730303
CDS Mutation	c.212C>T
AA Mutation	p.Pro71Leu(p.P71L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155015439:155015439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765952788
CDS Mutation	c.1580T>C
AA Mutation	p.Val527Ala(p.V527A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155014074:155014074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.215T>A
AA Mutation	p.Leu72His(p.L72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155014221:155014221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362T>G
AA Mutation	p.Leu121Arg(p.L121R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155017416:155017416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3557C>T
AA Mutation	p.Ala1186Val(p.A1186V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155016879:155016879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3020C>A
AA Mutation	p.Pro1007His(p.P1007H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000435029
Start	155014699:155014699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.840C>A
AA Mutation	p.Asp280Glu(p.D280E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435029
Start	155015570:155015570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1711C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435029
Start	155016479:155016479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2620C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435029
Start	155017417:155017417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3558T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000435029
Start	155015071:155015071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000435029
Start	155015526:155015527(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1667_1668insTCTG
AA Mutation	p.Gln556HisfsTer6(p.Q556Hfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript