Product Details

SNP ID
rs76490277
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:109647244 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTTTCTTATCAATGTATGTCAGC[A/C]TGTGTAGCTCAGTGGTAAAGCACAT
Phenotype
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
PALM2 PubMed Links

Gene Details

Gene
PALM2
Gene Name
paralemmin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001037293.2 Intron NP_001032370.1
NM_053016.5 Intron NP_443749.5

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