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SNP ID

rs143009356

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:69744907 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGGGGGTTCAGCACCTTGGGGTTG[C/G]GGGAGAAGTGCATGTGCAGGGTGCC

Phenotype

MIM: 613586

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NOB1 PubMed Links

Gene Details

Gene

NOB1

Gene Name

NIN1/PSMD8 binding protein 1 homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014062.2		Intron			NP_054781.1

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