Product Details

SNP ID

hCV25642602

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:81116416 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTGATTAAATGGTCACAATTATT[C/T]TACCAGCTGTTGTAATAATTTATGC

Phenotype

MIM: 300385

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HMGN5 PubMed Links

Gene Details

Gene

HMGN5

Gene Name

high mobility group nucleosome binding domain 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030763.2		Intron			NP_110390.1

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