Product Details

SNP ID

rs116156022

Assay Type

Functionally tested

NCBI dbSNP Submissions

30

Location

Chr.1:153438322 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAACATGACTTTCTCACCTAGAGGG[A/G]TATTCATCTTTGCTTTCAAAAAGCC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

S100A7L2 PubMed Links

Gene Details

Gene

S100A7L2

Gene Name

S100 calcium binding protein A7 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001045479.1	119	Missense Mutation	ACC,ATC	T14I	NP_001038944.2

View Full Product Details