Product Details

SNP ID

rs34162779

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:122775477 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGAACCGAGCATTGCAGCGGCGCT[G/T]TCCCAGCTCAGCTGGCCTTCCTCGG

Phenotype

MIM: 605929

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SNX2 PubMed Links

Gene Details

Gene

SNX2

Gene Name

sorting nexin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001278199.1	482	UTR 5			NP_001265128.1
NM_003100.3	482	Intron			NP_003091.2

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