Mutation

Primary Site >> Stomach Cancer

Gene >> KIF4A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70290496:70290496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38C>T
AA Mutation	p.Ala13Val(p.A13V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70419682:70419682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772078243
CDS Mutation	c.3394C>T
AA Mutation	p.Arg1132Trp(p.R1132W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70406921:70406921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3101T>C
AA Mutation	p.Phe1034Ser(p.F1034S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70301934:70301934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551C>T
AA Mutation	p.Ala184Val(p.A184V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70386621:70386621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2038C>T
AA Mutation	p.Arg680Cys(p.R680C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70395976:70395976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200516198
CDS Mutation	c.2416C>T
AA Mutation	p.Arg806Cys(p.R806C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70299152:70299152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466C>T
AA Mutation	p.Arg156Cys(p.R156C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374403
Start	70417925:70417925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3293G>T
AA Mutation	p.Gly1098Val(p.G1098V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374403
Start	70420079:70420079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3513C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374403
Start	70297125:70297126(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.363_364insAGATTGCT
AA Mutation	p.Leu122ArgfsTer18(p.L122Rfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript