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SNP ID

rs16861629

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:187121427 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAAGACAAGAAAGAGGATCTTTAG[A/T]GCCACAGCGAGGGCTCATTGCCACT

Phenotype

MIM: 607547

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

RPL39L PubMed Links

Gene Details

Gene

RPL39L

Gene Name

ribosomal protein L39 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052969.1		Intron			NP_443201.1

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