Product Details

SNP ID

rs9969708

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:37887665 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTAACTGATGGTTTTTTCATATAA[A/C]CTTTAACAAGAACTCATAAGTTGCA

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC25A51 PubMed Links

Gene Details

Gene

SLC25A51

Gene Name

solute carrier family 25 member 51

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033412.3	1336	Missense Mutation	GTT,TTT	V296F	NP_219480.1

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