Mutation

Primary Site >> Stomach Cancer

Gene >> QKI

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163455391:163455391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255A>C
AA Mutation	p.Lys85Asn(p.K85N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163563485:163563485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773954748
CDS Mutation	c.700C>T
AA Mutation	p.Pro234Ser(p.P234S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163415197:163415197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4G>T
AA Mutation	p.Val2Phe(p.V2F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163535069:163535069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490G>A
AA Mutation	p.Ala164Thr(p.A164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163563423:163563423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638C>G
AA Mutation	p.Ala213Gly(p.A213G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163566756:163566756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Cys(p.R324C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163563687:163563687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902T>G
AA Mutation	p.Leu301Arg(p.L301R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361752
Start	163563510:163563510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142647102
CDS Mutation	c.725G>A
AA Mutation	p.Arg242His(p.R242H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163563535:163563535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778641586
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163563484:163563484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764441206
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361752
Start	163478809:163478809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361752
Start	163478888:163478888(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755727862
CDS Mutation	c.401delA
AA Mutation	p.Lys134ArgfsTer14(p.K134Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361752
Start	163478887:163478888(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs766110096
CDS Mutation	c.401dupA
AA Mutation	p.Glu135GlyfsTer5(p.E135Gfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000361752
Start	163455277:163455278(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.143-1_143delGA
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	15
Mutation Consequence	start_lost
Transcription ID	ENST00000361752
Start	163415196:163415196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript