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SNP ID

rs116285916

Assay Type

Functionally tested

NCBI dbSNP Submissions

10

Location

Chr.1:10014901 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCGTGAGACTGCATCCTTAACCT[A/G]TGCAGTCTGTGCTAACTCTGGGTAG

Phenotype

MIM: 608604

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RBP7 PubMed Links

Gene Details

Gene

RBP7

Gene Name

retinol binding protein 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052960.2		Intron			NP_443192.1

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