Product Details

SNP ID

rs150876475

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:30399717 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTATTTTCTCCTGCGTTGGCTCCG[A/C]GGTGAGGGAAGAGGGGCTGCGGGAG

Phenotype

MIM: 607558

Polymorphism

A/C, Transversion 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	305	Silent Mutation	CGA,CGC	R43R	NP_001191133.1
NM_001291932.1	305	Intron			NP_001278861.1
NM_012429.4	305	Silent Mutation	CGA,CGC	R43R	NP_036561.1
NM_033382.2	305	Silent Mutation	CGA,CGC	R43R	NP_203740.1

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