Product Details

SNP ID

rs1418387

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:92690255 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACTCCGCCGCCGCGCTGGCCGCTG[C/T]CTACGGACCCGGCGGCTTCGGGGGC

Phenotype

MIM: 604420

Polymorphism

C/T, Transition 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	332	Missense Mutation	GCC,GTC	A90V	NP_002720.1

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