Mutation

Primary Site >> Stomach Cancer

Gene >> NR4A2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329609:156329609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759305222
CDS Mutation	c.578G>A
AA Mutation	p.Arg193His(p.R193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156326276:156326276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414A>T
AA Mutation	p.Arg472Trp(p.R472W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156325827:156325827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714C>T
AA Mutation	p.Arg572Cys(p.R572C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329604:156329604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583G>A
AA Mutation	p.Asp195Asn(p.D195N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156328506:156328506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773502234
CDS Mutation	c.892G>A
AA Mutation	p.Val298Met(p.V298M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329469:156329469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718G>A
AA Mutation	p.Ala240Thr(p.A240T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329984:156329984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203G>T
AA Mutation	p.Ser68Ile(p.S68I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156328464:156328464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Trp(p.R312W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156328008:156328008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001G>A
AA Mutation	p.Arg334His(p.R334H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156326742:156326742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1337T>C
AA Mutation	p.Leu446Pro(p.L446P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329685:156329685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502A>G
AA Mutation	p.Thr168Ala(p.T168A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156326183:156326183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507T>C
AA Mutation	p.Phe503Leu(p.F503L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156328501:156328501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156329929:156329929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156328007:156328007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156325927:156325927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550135305
CDS Mutation	c.1614C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156328528:156328528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156329362:156329362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339562
Start	156329862:156329862(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.325delC
AA Mutation	p.Gln109SerfsTer5(p.Q109Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339562
Start	156328517:156328517(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.881delA
AA Mutation	p.Asn294MetfsTer7(p.N294Mfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000339562
Start	156329950:156329950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237C>A
AA Mutation	p.Tyr79Ter(p.Y79*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339562
Start	156328516:156328517(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.881dupA
AA Mutation	p.Asn294LysfsTer10(p.N294Kfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript