Mutation

Primary Site >> Stomach Cancer

Gene >> KIF2A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62363705:62363705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273C>G
AA Mutation	p.Gln425Glu(p.Q425E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62348157:62348157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269A>C
AA Mutation	p.Lys90Thr(p.K90T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62358202:62358202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.775C>T
AA Mutation	p.Pro259Ser(p.P259S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62373709:62373709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669C>A
AA Mutation	p.Pro557Thr(p.P557T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62363733:62363733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301G>A
AA Mutation	p.Arg434Gln(p.R434Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000401507
Start	62347151:62347151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86T>C
AA Mutation	p.Val29Ala(p.V29A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401507
Start	62347173:62347173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401507
Start	62363842:62363842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754391420
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000401507
Start	62352688:62352688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.440delA
AA Mutation	p.Lys147ArgfsTer14(p.K147Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000401507
Start	62381251:62381251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2035+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000401507
Start	62373694:62373694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654G>T
AA Mutation	p.Glu552Ter(p.E552*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript