Product Details

SNP ID

rs142599505

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:137753730 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACTGCGAGAAGTGCTCGATCAGGT[C/G]GCCCTCAGCCACGTCTCCTTTAAGG

Phenotype

MIM: 609409

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

HNRNPA0 PubMed Links

Gene Details

Gene

HNRNPA0

Gene Name

heterogeneous nuclear ribonucleoprotein A0

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006805.3	621	Missense Mutation	CAC,GAC	H113D	NP_006796.1

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