Product Details

SNP ID

rs11696758

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:17946359 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAAAAAGAACCCTGGCTCCTTGAA[A/G]AAATGGCCAGTTTCAAGGCTGGAGC

Phenotype

MIM: 605937

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SNX5 PubMed Links

Gene Details

Gene

SNX5

Gene Name

sorting nexin 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282454.1		Intron			NP_001269383.1
NM_014426.3		Intron			NP_055241.1
NM_152227.2		Intron			NP_689413.1

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