Product Details

SNP ID

hCV89715765

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:82356797 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGTAAACTTAGGCTCTAGCTTACC[A/G]CCACCTCTTCCACGAGCTCTTCCTG

Phenotype

MIM: 601324

Polymorphism

A/G, 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	1170	Silent Mutation	GGC,GGT	G265G	NP_001003810.1
NM_002138.3	1170	Silent Mutation	GGC,GGT	G284G	NP_002129.2
NM_031369.2	1170	Silent Mutation	GGC,GGT	G265G	NP_112737.1
NM_031370.2	1170	Silent Mutation	GGC,GGT	G284G	NP_112738.1

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