Product Details

SNP ID

rs141106646

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:153373864 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGTGGTAATGGGCAGCCTTCAGC[A/G]CAATGGCTACCAGGGATATGAATTC

Phenotype

MIM: 603112

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

S100A12 PubMed Links

Gene Details

Gene

S100A12

Gene Name

S100 calcium binding protein A12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005621.1	310	Missense Mutation	GCG,GTG	A81V	NP_005612.1

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