Mutation

Primary Site >> Stomach Cancer

Gene >> DIDO1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62879795:62879795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6161C>T
AA Mutation	p.Ala2054Val(p.A2054V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62894451:62894451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374708890
CDS Mutation	c.2534G>A
AA Mutation	p.Arg845His(p.R845H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62880006:62880006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5950C>T
AA Mutation	p.Pro1984Ser(p.P1984S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62910991:62910991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746361252
CDS Mutation	c.622A>G
AA Mutation	p.Thr208Ala(p.T208A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62896781:62896781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138811075
CDS Mutation	c.1804G>A
AA Mutation	p.Ala602Thr(p.A602T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62881739:62881739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4217G>A
AA Mutation	p.Arg1406Gln(p.R1406Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62881271:62881271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4685A>T
AA Mutation	p.Gln1562Leu(p.Q1562L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62879864:62879864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6092G>A
AA Mutation	p.Ser2031Asn(p.S2031N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62894449:62894449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2536G>T
AA Mutation	p.Ala846Ser(p.A846S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62882042:62882042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762356761
CDS Mutation	c.3914C>T
AA Mutation	p.Ser1305Leu(p.S1305L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62911426:62911426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187C>A
AA Mutation	p.Arg63Ser(p.R63S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62879577:62879577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6379C>T
AA Mutation	p.Arg2127Trp(p.R2127W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62891074:62891074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3427C>T
AA Mutation	p.Arg1143Cys(p.R1143C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62909917:62909917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943A>G
AA Mutation	p.Ile315Val(p.I315V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62911048:62911048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769538311
CDS Mutation	c.565C>T
AA Mutation	p.Arg189Trp(p.R189W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62911156:62911156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457G>A
AA Mutation	p.Asp153Asn(p.D153N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62879660:62879660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6296C>A
AA Mutation	p.Pro2099Gln(p.P2099Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62896696:62896696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1889G>A
AA Mutation	p.Gly630Asp(p.G630D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62879909:62879909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6047C>T
AA Mutation	p.Pro2016Leu(p.P2016L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62881776:62881776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4180G>A
AA Mutation	p.Glu1394Lys(p.E1394K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62895144:62895144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779511231
CDS Mutation	c.2236C>T
AA Mutation	p.Arg746Cys(p.R746C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62879630:62879630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6326C>T
AA Mutation	p.Ala2109Val(p.A2109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62881605:62881605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746238090
CDS Mutation	c.4351G>T
AA Mutation	p.Asp1451Tyr(p.D1451Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62909982:62909982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878A>G
AA Mutation	p.His293Arg(p.H293R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62881406:62881406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778919517
CDS Mutation	c.4550C>T
AA Mutation	p.Ser1517Leu(p.S1517L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62882171:62882171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756232019
CDS Mutation	c.3785C>T
AA Mutation	p.Pro1262Leu(p.P1262L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62881526:62881526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4430A>C
AA Mutation	p.Lys1477Thr(p.K1477T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62881698:62881698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4258G>A
AA Mutation	p.Glu1420Lys(p.E1420K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62882045:62882045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3911C>T
AA Mutation	p.Ala1304Val(p.A1304V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000266070
Start	62893874:62893874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2893G>T
AA Mutation	p.Gly965Cys(p.G965C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62910821:62910821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548961303
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62880709:62880709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5247G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62881435:62881435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4521C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62882395:62882395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760224789
CDS Mutation	c.3561G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62881402:62881402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756935492
CDS Mutation	c.4554C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62881090:62881090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4866C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62881963:62881963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3993C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62911367:62911367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62907156:62907156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146285634
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62881507:62881507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4449C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266070
Start	62881405:62881405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4551G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266070
Start	62879588:62879589(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6367_6368delTG
AA Mutation	p.Trp2123GlufsTer133(p.W2123Efs*133)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266070
Start	62879855:62879855(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6101delC
AA Mutation	p.Pro2034ArgfsTer240(p.P2034Rfs*240)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266070
Start	62880722:62880722(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5234delG
AA Mutation	p.Gly1745AlafsTer119(p.G1745Afs*119)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266070
Start	62880233:62880233(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5723delC
AA Mutation	p.Pro1908LeufsTer111(p.P1908Lfs*111)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	46
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266070
Start	62880460:62880461(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5495_5496insACTGCGGGGATCTCGTGGTGGGAACTGTGTCTGTTTTC
AA Mutation	p.Gly1833LeufsTer44(p.G1833Lfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266070
Start	62882133:62882134(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3822dupA
AA Mutation	p.Val1275SerfsTer100(p.V1275Sfs*100)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript