Product Details

SNP ID

rs184882393

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:92694656 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATAAAGGTGCTTCTTTGGATAGCT[C/G]TCAATGTTCGCCCTCCCCTGCCTCC

Phenotype

MIM: 604420

Polymorphism

C/G, 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	764	Missense Mutation	TCT,TGT	S234C	NP_002720.1

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