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SNP ID

rs78924001

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:137751991 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGATGGCAAAACTTCCAAATCTGA[C/T]GCAATTGTCTTAAGCAAGTTTTTAA

Phenotype

MIM: 609409

Polymorphism

C/T, Transition 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	2360	UTR 3			NP_006796.1

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