Mutation

Primary Site >> Stomach Cancer

Gene >> NID2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52067874:52067874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518C>T
AA Mutation	p.Ala173Val(p.A173V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52068883:52068883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112C>T
AA Mutation	p.Pro38Ser(p.P38S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52019149:52019149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2940C>A
AA Mutation	p.Phe980Leu(p.F980L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52011614:52011614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374865918
CDS Mutation	c.3490C>T
AA Mutation	p.Arg1164Trp(p.R1164W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52040660:52040660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2017T>C
AA Mutation	p.Ser673Pro(p.S673P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52067898:52067898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757781562
CDS Mutation	c.494C>T
AA Mutation	p.Ala165Val(p.A165V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52029559:52029559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758169329
CDS Mutation	c.2389C>T
AA Mutation	p.Arg797Trp(p.R797W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52010916:52010916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3682C>G
AA Mutation	p.Leu1228Val(p.L1228V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52054197:52054197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147980330
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Cys(p.R298C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52053701:52053701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1307C>T
AA Mutation	p.Pro436Leu(p.P436L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000216286
Start	52010961:52010961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370703062
CDS Mutation	c.3637G>A
AA Mutation	p.Ala1213Thr(p.A1213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216286
Start	52042268:52042268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763461550
CDS Mutation	c.1662G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216286
Start	52027325:52027325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532998760
CDS Mutation	c.2550C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216286
Start	52053757:52053757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776405624
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216286
Start	52011657:52011657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756293649
CDS Mutation	c.3447C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216286
Start	52042316:52042316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1614C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216286
Start	52038940:52038940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2064T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216286
Start	52015201:52015201(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3103delC
AA Mutation	p.Arg1035GlyfsTer67(p.R1035Gfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216286
Start	52042183:52042183(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1747delC
AA Mutation	p.Leu583SerfsTer14(p.L583Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216286
Start	52068002:52068002(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.390delC
AA Mutation	p.Ala131GlnfsTer33(p.A131Qfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000216286
Start	52040649:52040649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2026+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript