Product Details

SNP ID

rs2275729

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.10:92692673 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTGGCACGTCCCGACGCGGGCTCGT[G/T]GCAAGTTTTCTTTCTCTCTTTCCTG

Phenotype

MIM: 604420

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

HHEX PubMed Links

Gene Details

Gene

HHEX

Gene Name

hematopoietically expressed homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002729.4		Intron			NP_002720.1

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