Product Details

SNP ID

rs1389550

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:12291024 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAGTGGATGAAAATCTGAAGGCTA[C/G]ACACCCTGCAGGAAAATCTGAATGG

Phenotype

MIM: 612355

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

MICALCL PubMed Links

Gene Details

Gene

MICALCL

Gene Name

MICAL C-terminal like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032867.2		Intron			NP_116256.2

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