Product Details

SNP ID

rs10458913

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:44263723 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCATAGCAGGGCCTGGAGGCCGAGC[A/G]TGGCCACACGTCCTCTAGCAAAGCC

Phenotype

MIM: 605420

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ALX4 PubMed Links

Gene Details

Gene

ALX4

Gene Name

ALX homeobox 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021926.3	2471	UTR 3			NP_068745.2

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