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SNP ID

rs115711125

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:53942724 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATAAGGCAGCAGACAAAGAAAGGGG[A/G]CTTCTTTGAGAAGGCAAGACTGGAG

Phenotype

MIM: 142976

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

HOXC13 PubMed Links

Gene Details

Gene

HOXC13

Gene Name

homeobox C13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017410.2		Intron			NP_059106.2

Gene

HOXC13-AS

Gene Name

HOXC13 antisense RNA

There are no transcripts associated with this gene.

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