Colon Cancer: Gene >> NR4A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99863785:99863785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1799G>A
AA Mutation	p.Arg600His(p.R600H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99828250:99828250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208G>A
AA Mutation	p.Glu70Lys(p.E70K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99863623:99863623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637G>T
AA Mutation	p.Arg546Ile(p.R546I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99844707:99844707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313A>G
AA Mutation	p.Tyr438Cys(p.Y438C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99832797:99832797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060A>G
AA Mutation	p.Ser354Gly(p.S354G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99832707:99832707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970G>A
AA Mutation	p.Ala324Thr(p.A324T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99833411:99833411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778148069
CDS Mutation	c.1211G>A
AA Mutation	p.Arg404Gln(p.R404Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99828047:99828047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5C>A
AA Mutation	p.Pro2His(p.P2H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99847538:99847538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1556A>T
AA Mutation	p.Asp519Val(p.D519V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395097
Start	99844744:99844744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395097
Start	99863646:99863646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1660delA
AA Mutation	p.Arg554GlufsTer13(p.R554Efs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000395097
Start	99847536:99847537(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1554_1555insCAG
AA Mutation	p.Lys518_Asp519insGln(p.K518_D519insQ)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NR4A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99832765:99832765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028G>A
AA Mutation	p.Arg343Gln(p.R343Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99832780:99832780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043G>A
AA Mutation	p.Arg348Gln(p.R348Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395097
Start	99833380:99833380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180C>A
AA Mutation	p.Pro394Thr(p.P394T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395097
Start	99832739:99832739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript