Product Details

SNP ID

rs61742168

Assay Type

Functionally tested

NCBI dbSNP Submissions

23

Location

Chr.1:153438301 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGAAACATCGCGACTATGTCCAAC[A/G]TGACTTTCTCACCTAGAGGGATATT

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	140	Missense Mutation	ACG,ATG	T21M	NP_001038944.2

View Full Product Details