Product Details

SNP ID

rs5982097

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:73213947 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTCCTCATTACCATACATCTCTTC[A/G]TGACACATTTCCTCATCATCACAGT

Phenotype

MIM: 300026

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NAP1L2 PubMed Links

Gene Details

Gene

NAP1L2

Gene Name

nucleosome assembly protein 1 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021963.3	928	Silent Mutation	CAC,CAT	H182H	NP_068798.1

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