Mutation

Primary Site >> Stomach Cancer

Gene >> KIF23

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69435727:69435727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228A>G
AA Mutation	p.Ile410Val(p.I410V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69417459:69417459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158A>G
AA Mutation	p.Gln53Arg(p.Q53R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69440312:69440312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1892G>A
AA Mutation	p.Arg631His(p.R631H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69440942:69440942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747635090
CDS Mutation	c.2242C>T
AA Mutation	p.Arg748Cys(p.R748C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69440979:69440979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2279T>G
AA Mutation	p.Ile760Ser(p.I760S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69444827:69444827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763116733
CDS Mutation	c.2417G>A
AA Mutation	p.Arg806His(p.R806H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260363
Start	69440438:69440438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2018G>A
AA Mutation	p.Arg673Gln(p.R673Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260363
Start	69436580:69436580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747697382
CDS Mutation	c.1413C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260363
Start	69436616:69436616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260363
Start	69416025:69416025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.48delA
AA Mutation	p.Ser18ProfsTer27(p.S18Pfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000260363
Start	69435664:69435664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165C>T
AA Mutation	p.Arg389Ter(p.R389*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript