Product Details

SNP ID

rs11089450

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:30450657 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TACAAGTAAGACCTCTCCGTTTCAA[G/T]TTATGGGACCCTGGGCAAATTCCTT

Phenotype

MIM: 612824

Polymorphism

G/T, Transversion 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		Intron			NP_001244307.1
NM_001257379.1		Intron			NP_001244308.1
NM_001257382.1		Intron			NP_001244311.1
NM_174975.4		Intron			NP_777635.1
XM_011530128.2		Intron			XP_011528430.1

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