Product Details

SNP ID: rs7853479
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:74506768 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTTCAAATTTCCACATAGTGGGCA[A/G]GACCACAGAGTCATACCTTTTAAGT
Phenotype: MIM: 601972
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: RORB PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006914.3		Intron			NP_008845.2

There are no transcripts associated with this gene.