Mutation

Primary Site >> Stomach Cancer

Gene >> ZBTB20

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350750:114350750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328G>A
AA Mutation	p.Ser443Asn(p.S443N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351594:114351594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484G>A
AA Mutation	p.Val162Met(p.V162M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351008:114351008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760166000
CDS Mutation	c.1070C>T
AA Mutation	p.Thr357Met(p.T357M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114339241:114339241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1990T>C
AA Mutation	p.Cys664Arg(p.C664R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351507:114351507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571C>T
AA Mutation	p.Arg191Cys(p.R191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350549:114350549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1529C>T
AA Mutation	p.Ala510Val(p.A510V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350567:114350567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1511G>A
AA Mutation	p.Gly504Asp(p.G504D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351588:114351588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Trp(p.R164W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350931:114350931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147A>G
AA Mutation	p.Ile383Val(p.I383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351407:114351407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671G>T
AA Mutation	p.Ser224Ile(p.S224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351785:114351785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293G>A
AA Mutation	p.Arg98His(p.R98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351758:114351758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320C>T
AA Mutation	p.Thr107Met(p.T107M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350879:114350879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199G>A
AA Mutation	p.Arg400Gln(p.R400Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350411:114350411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667C>T
AA Mutation	p.Ala556Val(p.A556V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350667:114350667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1411C>A
AA Mutation	p.Pro471Thr(p.P471T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351198:114351198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Cys(p.R294C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350526:114350526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771958765
CDS Mutation	c.1552G>A
AA Mutation	p.Gly518Ser(p.G518S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114350646:114350646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432C>T
AA Mutation	p.Arg478Cys(p.R478C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000474710
Start	114351024:114351024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054G>A
AA Mutation	p.Glu352Lys(p.E352K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114351595:114351595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772400910
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114351391:114351391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114350764:114350764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1314A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114351718:114351718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763978377
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114350479:114350479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1599A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114351073:114351073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367805942
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114351259:114351259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114350866:114350866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114339011:114339011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780461943
CDS Mutation	c.2220C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114351331:114351331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114350932:114350932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1146C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114350881:114350881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1197G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114351598:114351598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000474710
Start	114339281:114339281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144019743
CDS Mutation	c.1950C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000474710
Start	114339156:114339156(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2075delC
AA Mutation	p.Pro692LeufsTer43(p.P692Lfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000474710
Start	114350351:114350351(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1727delA
AA Mutation	p.Lys576SerfsTer42(p.K576Sfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000474710
Start	114339120:114339120(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2111delC
AA Mutation	p.Pro704GlnfsTer31(p.P704Qfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript