Product Details

SNP ID

rs140989967

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:81120677 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGTGTTATACGGTTTTACCAAGCA[A/G]TGAAACAGCGTTCGATTTCACTTCT

Phenotype

MIM: 300385

Polymorphism

A/G, 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
XM_006724688.3		Intron			XP_006724751.1
XM_017029839.1		Intron			XP_016885328.1
XM_017029840.1		Intron			XP_016885329.1

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