Mutation

Primary Site >> Stomach Cancer

Gene >> NID1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	235993788:235993788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200827911
CDS Mutation	c.2612C>T
AA Mutation	p.Pro871Leu(p.P871L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	235981741:235981741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750240264
CDS Mutation	c.3097C>T
AA Mutation	p.Arg1033Cys(p.R1033C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236017246:236017246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2156C>T
AA Mutation	p.Ser719Leu(p.S719L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236038229:236038229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs16833154
CDS Mutation	c.1160G>A
AA Mutation	p.Arg387His(p.R387H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236024081:236024081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759141799
CDS Mutation	c.2117G>A
AA Mutation	p.Arg706Gln(p.R706Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	235985472:235985472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188200854
CDS Mutation	c.2962G>A
AA Mutation	p.Val988Met(p.V988M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236045517:236045517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692A>G
AA Mutation	p.Lys231Arg(p.K231R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236042276:236042276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.769C>A
AA Mutation	p.Gln257Lys(p.Q257K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236017156:236017156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2246C>T
AA Mutation	p.Thr749Met(p.T749M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236029639:236029639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767774351
CDS Mutation	c.1649C>T
AA Mutation	p.Thr550Met(p.T550M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	235979100:235979100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752565337
CDS Mutation	c.3517G>A
AA Mutation	p.Val1173Met(p.V1173M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236041958:236041958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087C>A
AA Mutation	p.Gln363Lys(p.Q363K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236048788:236048788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427C>T
AA Mutation	p.Pro143Ser(p.P143S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236011930:236011930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771612950
CDS Mutation	c.2518G>A
AA Mutation	p.Val840Met(p.V840M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236045470:236045470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739G>A
AA Mutation	p.Glu247Lys(p.E247K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236025983:236025983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897C>A
AA Mutation	p.Leu633Ile(p.L633I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236032554:236032554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111733802
CDS Mutation	c.1384G>A
AA Mutation	p.Val462Ile(p.V462I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	235980649:235980649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3232C>A
AA Mutation	p.Leu1078Ile(p.L1078I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236038124:236038124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265G>A
AA Mutation	p.Gly422Asp(p.G422D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236011927:236011927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2521C>T
AA Mutation	p.Pro841Ser(p.P841S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	235985397:235985397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3037A>G
AA Mutation	p.Thr1013Ala(p.T1013A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	235993705:235993705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748671846
CDS Mutation	c.2695G>A
AA Mutation	p.Val899Met(p.V899M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236025968:236025968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748178076
CDS Mutation	c.1912G>A
AA Mutation	p.Val638Met(p.V638M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000264187
Start	236064895:236064895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185C>T
AA Mutation	p.Ala62Val(p.A62V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264187
Start	236029716:236029716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264187
Start	235979854:235979854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115093040
CDS Mutation	c.3477C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264187
Start	235979065:235979065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546812606
CDS Mutation	c.3552G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264187
Start	235993745:235993745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2655G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264187
Start	236032519:236032519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1419C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264187
Start	236025963:236025963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767535442
CDS Mutation	c.1917C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264187
Start	235990939:235990939(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2875delC
AA Mutation	p.Leu959TrpfsTer6(p.L959Wfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000264187
Start	235981708:235981708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3130C>T
AA Mutation	p.Arg1044Ter(p.R1044*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000264187
Start	235981678:235981678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3160C>T
AA Mutation	p.Gln1054Ter(p.Q1054*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000264187
Start	236038153:236038153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1236C>A
AA Mutation	p.Cys412Ter(p.C412*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript