Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NR4A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329645:156329645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542C>T
AA Mutation	p.Ser181Leu(p.S181L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000339562
Start	156328532:156328532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866G>A
AA Mutation	p.Arg289His(p.R289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156328415:156328415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983T>C
AA Mutation	p.Met328Thr(p.M328T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329684:156329684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503C>T
AA Mutation	p.Thr168Met(p.T168M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156327969:156327969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1040C>T
AA Mutation	p.Ser347Leu(p.S347L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156330171:156330171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16G>A
AA Mutation	p.Ala6Thr(p.A6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156325926:156325926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201003462
CDS Mutation	c.1615G>A
AA Mutation	p.Val539Met(p.V539M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156327864:156327864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145T>G
AA Mutation	p.Leu382Arg(p.L382R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329973:156329973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Asp72Asn(p.D72N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156329345:156329345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842A>G
AA Mutation	p.Glu281Gly(p.E281G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156327908:156327908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1101C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156327968:156327968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756870590
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
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

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156329809:156329809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781377163
CDS Mutation	c.378G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339562
Start	156330169:156330169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752342124
CDS Mutation	c.18G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
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

Mutation ID	17
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

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339562
Start	156329599:156329599(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.588delG
AA Mutation	p.Leu198CysfsTer5(p.L198Cfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
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

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339562
Start	156329861:156329862(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs774629025
CDS Mutation	c.325dupC
AA Mutation	p.Gln109ProfsTer3(p.Q109Pfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NR4A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156328448:156328448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950A>G
AA Mutation	p.Tyr317Cys(p.Y317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339562
Start	156328011:156328011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998T>C
AA Mutation	p.Val333Ala(p.V333A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000339562
Start	156328532:156328532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866G>A
AA Mutation	p.Arg289His(p.R289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript