Product Details

SNP ID

rs66502635

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:1434361 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAAACACGGAGGCACGTAGGAGTC[C/T]GGGGCCATGTGGTCGGTTTCTTTAT

Phenotype

Polymorphism

C/T, Transition 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	3074	UTR 3			NP_891554.1
XM_011515520.2	3074	Missense Mutation	CAG,CGG	Q982R	XP_011513822.1
XM_011515522.2	3074	Missense Mutation	CAG,CGG	Q968R	XP_011513824.1
XM_011515523.2	3074	Missense Mutation	CAG,CGG	Q899R	XP_011513825.1
XM_011515524.2	3074	Missense Mutation	CAG,CGG	Q411R	XP_011513826.1
XM_017012619.1	3074	Intron			XP_016868108.1

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