Product Details

SNP ID

rs16900358

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:157716624 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTAGCATGAGCGATTTTACTTTGA[A/C]AATGTTCAAGCTTATATGGTTTTCT

Phenotype

MIM: 605952

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SNX9 PubMed Links

Gene Details

Gene

SNX9

Gene Name

sorting nexin 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016224.4		Intron			NP_057308.1
XM_005267015.2		Intron			XP_005267072.1
XM_011535886.2		Intron			XP_011534188.1

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