Mutation

Primary Site >> Stomach Cancer

Gene >> FOXK2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335255
Start	82586172:82586172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1548G>T
AA Mutation	p.Gln516His(p.Q516H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335255
Start	82571737:82571737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776C>T
AA Mutation	p.Pro259Leu(p.P259L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335255
Start	82571799:82571799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838A>G
AA Mutation	p.Thr280Ala(p.T280A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335255
Start	82563536:82563536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602C>T
AA Mutation	p.Thr201Met(p.T201M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335255
Start	82601343:82601343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748730980
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335255
Start	82563456:82563456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371316297
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335255
Start	82587220:82587220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770075489
CDS Mutation	c.1734C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335255
Start	82520071:82520071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335255
Start	82586046:82586046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1422C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335255
Start	82584108:82584108(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1204delC
AA Mutation	p.Leu402TrpfsTer35(p.L402Wfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335255
Start	82587216:82587216(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1733delA
AA Mutation	p.Asn578ThrfsTer16(p.N578Tfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript