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SNP ID

rs12589099

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:39238101 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAATCAGATTCAAAGACATGTGTTT[C/T]TGAGCAAATGAAGGGCTGAGTTGTT

Phenotype

MIM: 608001

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MIA2 PubMed Links

Gene Details

Gene

MIA2

Gene Name

melanoma inhibitory activity 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_054024.3		Intron			NP_473365.3

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