Product Details

SNP ID

rs201802808

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:99828563 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCATCGCACCCGGCCCGCTGCTGG[A/C]CCCGCCGATGAAGGCGGTCCCCACG

Phenotype

MIM: 600542

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

LOC101928438 PubMed Links

Gene Details

Gene

LOC101928438

Gene Name

uncharacterized LOC101928438

There are no transcripts associated with this gene.

Gene

NR4A3

Gene Name

nuclear receptor subfamily 4 group A member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006981.3	1182	Missense Mutation	GAC,GCC	D174A	NP_008912.2
NM_173199.2	1182	Missense Mutation	GAC,GCC	D174A	NP_775291.1
NM_173200.2	1182	Missense Mutation	GAC,GCC	D185A	NP_775292.1
XM_017015162.1	1182	Missense Mutation	GAC,GCC	D174A	XP_016870651.1

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