Product Details

SNP ID
rs142272939
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:82357407 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATAAAGCAGAACCCACGCCTCTTA[C/T]TGGTCTTGTTGTCCATGGGGAGCTC
Phenotype
MIM: 601324
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HNRNPD PubMed Links

Gene Details

Gene
HNRNPD
Gene Name
heterogeneous nuclear ribonucleoprotein D
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001003810.1 977 Missense Mutation AAT,AGT N201S NP_001003810.1
NM_002138.3 977 Missense Mutation AAT,AGT N220S NP_002129.2
NM_031369.2 977 Missense Mutation AAT,AGT N201S NP_112737.1
NM_031370.2 977 Missense Mutation AAT,AGT N220S NP_112738.1

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