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SNP ID

hCV26232499

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:15841734 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAAGTCAAAGATGGCACTGTCTTA[A/G]GAAATCTACTCTTTTCCACACAGAA

Phenotype

MIM: 300629

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

AP1S2 PubMed Links

Gene Details

Gene

AP1S2

Gene Name

adaptor related protein complex 1 sigma 2 subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001272071.1		Intron			NP_001259000.1
NM_003916.4		Intron			NP_003907.3

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