Product Details

SNP ID
rs9606730
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:30448273 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTACCCCCCCAATGCCTCTGACC[C/T]CTGGGGTCCCTTGCTCCTTCCCCCA
Phenotype
MIM: 612824
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SEC14L3 PubMed Links

Gene Details

Gene
SEC14L3
Gene Name
SEC14 like lipid binding 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001257378.1 2110 Intron NP_001244307.1
NM_001257379.1 2110 Intron NP_001244308.1
NM_001257382.1 2110 Intron NP_001244311.1
NM_174975.4 2110 Intron NP_777635.1
XM_011530128.2 2110 UTR 3 XP_011528430.1

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