Product Details

SNP ID

rs139636778

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:30398396 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGACCTAGGCAAGGGGCAGAGGT[A/G]GCCAGTCCTCATTAGTGTCCTCTGG

Phenotype

MIM: 607558

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SEC14L2 PubMed Links

Gene Details

Gene

SEC14L2

Gene Name

SEC14 like lipid binding 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204204.2		Intron			NP_001191133.1
NM_001291932.1		Intron			NP_001278861.1
NM_012429.4		Intron			NP_036561.1
NM_033382.2		Intron			NP_203740.1

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