Mutation

Primary Site >> Stomach Cancer

Gene >> ZEB2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399923:144399923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141793065
CDS Mutation	c.1264G>A
AA Mutation	p.Ala422Thr(p.A422T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144400240:144400240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947A>G
AA Mutation	p.Lys316Arg(p.K316R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399733:144399733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1454A>C
AA Mutation	p.Lys485Thr(p.K485T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399755:144399755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432T>G
AA Mutation	p.Cys478Gly(p.C478G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144396584:144396584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2895G>T
AA Mutation	p.Leu965Phe(p.L965F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399118:144399118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2069A>G
AA Mutation	p.Glu690Gly(p.E690G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399538:144399538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1649A>G
AA Mutation	p.Gln550Arg(p.Q550R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144398675:144398675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2512A>C
AA Mutation	p.Lys838Gln(p.K838Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399994:144399994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193A>G
AA Mutation	p.Asn398Ser(p.N398S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144396516:144396516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776367143
CDS Mutation	c.2963G>A
AA Mutation	p.Arg988His(p.R988H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399646:144399646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541C>T
AA Mutation	p.Pro514Leu(p.P514L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144398647:144398647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2540A>C
AA Mutation	p.Asn847Thr(p.N847T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144424814:144424814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs730881187
CDS Mutation	c.385G>A
AA Mutation	p.Ala129Thr(p.A129T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144398638:144398638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529220318
CDS Mutation	c.2549C>T
AA Mutation	p.Ser850Phe(p.S850F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399154:144399154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2033C>T
AA Mutation	p.Ser678Phe(p.S678F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144404874:144404874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554G>A
AA Mutation	p.Arg185His(p.R185H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144399509:144399509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs730881194
CDS Mutation	c.1678C>T
AA Mutation	p.Arg560Cys(p.R560C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144398584:144398584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2603A>T
AA Mutation	p.Glu868Val(p.E868V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144404863:144404863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565C>T
AA Mutation	p.Pro189Ser(p.P189S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144398603:144398603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2584T>G
AA Mutation	p.Leu862Val(p.L862V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144389630:144389630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776351453
CDS Mutation	c.3466G>T
AA Mutation	p.Gly1156Cys(p.G1156C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000409487
Start	144398984:144398984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144154908
CDS Mutation	c.2203C>T
AA Mutation	p.Pro735Ser(p.P735S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144399069:144399069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2118A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144398481:144398481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754727621
CDS Mutation	c.2706C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144389535:144389535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3561T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144399189:144399189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1998C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144404021:144404021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140169964
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144396419:144396419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3060A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144404909:144404909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144398637:144398637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2550T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144398603:144398603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2584T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409487
Start	144399009:144399009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2178T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000409487
Start	144517320:144517320(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.31delC
AA Mutation	p.Arg11GlyfsTer16(p.R11Gfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000409487
Start	144398585:144398585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2602G>T
AA Mutation	p.Glu868Ter(p.E868*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000409487
Start	144429769:144429769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331G>T
AA Mutation	p.Glu111Ter(p.E111*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript