Product Details

SNP ID
rs200156703
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:1435116 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCCAGTCACCCAGCTTCTCAATCA[G/T]GTCCCGCAGCATCTGATCCTCCTCT
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
MICALL2 PubMed Links

Gene Details

Gene
MICALL2
Gene Name
MICAL like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_182924.3 2800 Missense Mutation NP_891554.1
XM_011515520.2 2800 Missense Mutation XP_011513822.1
XM_011515522.2 2800 Intron XP_011513824.1
XM_011515523.2 2800 Missense Mutation XP_011513825.1
XM_011515524.2 2800 Missense Mutation XP_011513826.1
XM_017012619.1 2800 Intron XP_016868108.1

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