Product Details

SNP ID

rs976025748

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:17789732 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGTCGCGTAGGACGCACCAGATG[C/T]CGCTGTGGCTCCCGCACCCGGGCGC

Phenotype

MIM: 608882

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MICAL3 PubMed Links

Gene Details

Gene

MICAL3

Gene Name

microtubule associated monooxygenase, calponin and LIM domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122731.2	7362	Intron			NP_001116203.1
NM_001136004.3	7362	Intron			NP_001129476.1
NM_015241.2	7362	UTR 3			NP_056056.2

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