Product Details

SNP ID: rs200753134
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:137753980 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCACGCAGTCCGTCAGAGTCCCAAA[A/G]GCCTCAAAGTGGCCGCGCAGGCCCG
Phenotype: MIM: 609409
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: HNRNPA0 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006805.3	371	Silent Mutation	GCC,GCT	A29A	NP_006796.1